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<script type="text/javascript" src="/corehtml/pmc/jatsreader/ptpmc_3.22/js/jr.boots.min.js"> </script><title>Zellweger Spectrum Disorder - GeneReviews® - NCBI Bookshelf</title>
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<meta name="citation_inbook_title" content="GeneReviews® [Internet]">
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<meta name="citation_title" content="Zellweger Spectrum Disorder">
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<meta name="citation_publisher" content="University of Washington, Seattle">
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<meta name="citation_date" content="2020/10/29">
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<meta name="citation_author" content="Steven J Steinberg">
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<meta name="citation_author" content="Gerald V Raymond">
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<meta name="citation_author" content="Nancy E Braverman">
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<meta name="citation_author" content="Ann B Moser">
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<meta name="citation_pmid" content="20301621">
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<meta name="citation_fulltext_html_url" content="https://www.ncbi.nlm.nih.gov/books/NBK1448/">
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<meta name="citation_keywords" content="ZSD">
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<meta name="citation_keywords" content="Intermediate/Milder Zellweger Spectrum Disorder (Neonatal Adrenoleukodystrophy, Infantile Refsum Disease, Heimler Syndrome)">
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<meta name="citation_keywords" content="Severe Zellweger Spectrum Disorder (Zellweger Syndrome)">
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<meta name="citation_keywords" content="Peroxisomal ATPase PEX1">
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<meta name="citation_keywords" content="Peroxisomal ATPase PEX6">
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<meta name="citation_keywords" content="Peroxisomal biogenesis factor 19">
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<meta name="citation_keywords" content="Peroxisomal biogenesis factor 3">
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<meta name="citation_keywords" content="Peroxisomal membrane protein 11B">
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<meta name="citation_keywords" content="Peroxisomal membrane protein PEX13">
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<meta name="citation_keywords" content="Peroxisomal membrane protein PEX14">
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<meta name="citation_keywords" content="Peroxisomal membrane protein PEX16">
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<meta name="citation_keywords" content="Peroxisomal targeting signal 1 receptor">
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<meta name="citation_keywords" content="Peroxisome assembly protein 12">
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<meta name="citation_keywords" content="Peroxisome assembly protein 26">
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<meta name="citation_keywords" content="Peroxisome biogenesis factor 10">
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<meta name="citation_keywords" content="Peroxisome biogenesis factor 2">
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<meta name="citation_keywords" content="PEX1">
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<meta name="citation_keywords" content="PEX10">
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<meta name="citation_keywords" content="PEX11B">
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<meta name="citation_keywords" content="PEX13">
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<meta name="citation_keywords" content="PEX14">
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<meta name="citation_keywords" content="PEX16">
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<meta name="citation_keywords" content="PEX19">
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<meta name="citation_keywords" content="PEX2">
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<meta name="citation_keywords" content="PEX26">
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<meta name="citation_keywords" content="PEX5">
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<meta name="citation_keywords" content="PEX6">
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<meta name="citation_keywords" content="Zellweger Spectrum Disorder (ZSD)">
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<meta name="DC.Title" content="Zellweger Spectrum Disorder">
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<meta name="DC.Publisher" content="University of Washington, Seattle">
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<meta name="DC.Contributor" content="Steven J Steinberg">
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<meta name="DC.Contributor" content="Gerald V Raymond">
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<meta name="DC.Contributor" content="Nancy E Braverman">
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<meta name="DC.Contributor" content="Ann B Moser">
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<meta name="DC.Date" content="2020/10/29">
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<meta name="description" content='Zellweger spectrum disorder (ZSD) is a phenotypic continuum ranging from severe to mild. While individual phenotypes (e.g., Zellweger syndrome [ZS], neonatal adrenoleukodystrophy [NALD], and infantile Refsum disease [IRD]) were described in the past before the biochemical and molecular bases of this spectrum were fully determined, the term "ZSD" is now used to refer to all individuals with a defect in one of the ZSD-PEX genes regardless of phenotype.'>
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<meta name="og:description" content='Zellweger spectrum disorder (ZSD) is a phenotypic continuum ranging from severe to mild. While individual phenotypes (e.g., Zellweger syndrome [ZS], neonatal adrenoleukodystrophy [NALD], and infantile Refsum disease [IRD]) were described in the past before the biochemical and molecular bases of this spectrum were fully determined, the term "ZSD" is now used to refer to all individuals with a defect in one of the ZSD-PEX genes regardless of phenotype.'>
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class="wsprkl btn" title="Jump to next match">▶</a></nav></nav></div><div id="jr-epub-interstitial" class="hidden"></div><div id="jr-content"><article data-type="main"><div class="main-content lit-style" itemscope="itemscope" itemtype="http://schema.org/CreativeWork"><div class="meta-content fm-sec"><div class="fm-sec"><h1 id="_NBK1448_"><span class="title" itemprop="name">Zellweger Spectrum Disorder</span></h1><div itemprop="alternativeHeadline" class="subtitle whole_rhythm">Synonym: ZSD</div><p class="contribs">Steinberg SJ, Raymond GV, Braverman NE, et al.</p><p class="fm-aai"><a href="#_NBK1448_pubdet_">Publication Details</a></p><p><em>Estimated reading time: 32 minutes</em></p></div></div><div class="jig-ncbiinpagenav body-content whole_rhythm" data-jigconfig="allHeadingLevels: ['h2'],smoothScroll: false" itemprop="text"><div id="pbd.Summary" itemprop="description"><h2 id="_pbd_Summary_">Summary</h2><div><h4 class="inline">Clinical characteristics.</h4><p>Zellweger spectrum disorder (ZSD) is a phenotypic continuum ranging from severe to mild. While individual phenotypes (e.g., Zellweger syndrome [ZS], neonatal adrenoleukodystrophy [NALD], and infantile Refsum disease [IRD]) were described in the past before the biochemical and molecular bases of this spectrum were fully determined, the term "ZSD" is now used to refer to all individuals with a defect in one of the ZSD-PEX genes regardless of phenotype.</p><p>Individuals with ZSD usually come to clinical attention in the newborn period or later in childhood. Affected newborns are hypotonic and feed poorly. They have distinctive facies, congenital malformations (neuronal migration defects associated with neonatal-onset seizures, renal cysts, and bony stippling [chondrodysplasia punctata] of the patella[e] and the long bones), and liver disease that can be severe. Infants with severe ZSD are significantly impaired and typically die during the first year of life, usually having made no developmental progress.</p><p>Individuals with intermediate/milder ZSD do not have congenital malformations, but rather progressive peroxisome dysfunction variably manifest as sensory loss (secondary to retinal dystrophy and sensorineural hearing loss), neurologic involvement (ataxia, polyneuropathy, and leukodystrophy), liver dysfunction, adrenal insufficiency, and renal oxalate stones. While hypotonia and developmental delays are typical, intellect can be normal. Some have osteopenia; almost all have ameleogenesis imperfecta in the secondary teeth.</p></div><div><h4 class="inline">Diagnosis/testing.</h4><p>The diagnosis of ZSD is established in a proband with the suggestive clinical and biochemical findings above by identification of biallelic pathogenic variants in one of the 13 known ZSD-PEX genes. One <i>PEX6</i> variant, p.Arg860Trp, has been associated with ZSD in the heterozygous state due to allelic expression imbalance dependent on allelic background.</p></div><div><h4 class="inline">Management.</h4><p><i>Treatment of manifestations:</i> The focus is on symptomatic therapy and may include gastrostomy to provide adequate calories, hearing aids, cataract removal, glasses to correct refractive errors, supplementation of fat-soluble vitamins, and cholic acid supplementation; varices can be treated with sclerosing therapies; anti-seizure medication, early intervention services for developmental delay and intellectual disability; adrenal replacement therapy; vitamin D supplementation and consideration of bisphosphonates for osteopenia; treatment as per dentist for ameliogenesis imperfecta. Supportive treatment for renal oxalate stones has included hydration, lithotripsy, and surgical intervention. Annual influenza and respiratory syncytial virus vaccines should be provided.</p><p><i>Surveillance</i>: Growth and nutrition should be assessed at each visit. Annual audiology and ophthalmologic evaluations; annual monitoring of liver function and coagulation factors, and ultrasound and/or fibroscan to evaluate liver architecture; monitor for changes in seizure activity; head MRI to evaluate for white matter changes that may explain changes in cognitive and/or motor ability; monitor developmental progress and educational needs; ACTH and cortisol levels by age one year and annually thereafter. Dental examinations every six months. Annual urine oxalate-to-creatinine ratio with consideration of renal imaging when performing liver imaging. Assessment of family needs at each visit.</p></div><div><h4 class="inline">Genetic counseling.</h4><p>ZSD is typically inherited in an autosomal recessive manner (one <i>PEX6</i> variant, p.Arg860Trp, has been associated with ZSD in the heterozygous state). At conception, each sib of an individual with biallelic ZSD-causing pathogenic variants has a 25% chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and not a carrier. Carrier testing for at-risk relatives is possible if the pathogenic variants have been identified in an affected family member. Prenatal testing for a pregnancy at increased risk is possible by DNA testing if both ZSD-related pathogenic variants have been identified in an affected family member, or by biochemical testing if the biochemical defects have been confirmed in cultured fibroblasts from an affected family member.</p></div></div><div id="pbd.GeneReview_Scope"><h2 id="_pbd_GeneReview_Scope_"><i>GeneReview</i> Scope</h2><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTc"><a href="/books/NBK1448/table/pbd.Tc/?report=objectonly" target="object" title="Table" class="img_link icnblk_img" rid-ob="figobpbdTc"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.Tc"><a href="/books/NBK1448/table/pbd.Tc/?report=objectonly" target="object" rid-ob="figobpbdTc">Table</a></h4><p class="float-caption no_bottom_margin">Severe ZSD (previously called Zellweger syndrome) Intermediate/milder ZSD (previously called neonatal adrenoleukodystrophy, infantile Refsum disease, or Heimler syndrome)</p></div></div></div><div id="pbd.Diagnosis"><h2 id="_pbd_Diagnosis_">Diagnosis</h2><div id="pbd.Suggestive_Findings"><h3>Suggestive Findings</h3><p>Zellweger spectrum disorder (ZSD) <b>should be suspected</b> in children with the following <a href="#pbd.Clinical_Findings">clinical</a> and <a href="#pbd.Laboratory_Findings">laboratory</a> findings.</p><div id="pbd.Clinical_Findings"><h4>Clinical Findings</h4><p>In newborns:</p><ul><li class="half_rhythm"><div>Hypotonia</div></li><li class="half_rhythm"><div>Poor feeding</div></li><li class="half_rhythm"><div>Distinctive facies</div></li><li class="half_rhythm"><div>Brain malformations</div></li><li class="half_rhythm"><div>Seizures</div></li><li class="half_rhythm"><div>Renal cysts</div></li><li class="half_rhythm"><div>Hepatomegaly, cholestasis, and hepatic dysfunction</div></li><li class="half_rhythm"><div>Bony stippling (chondrodysplasia punctata) of the patella(e) and other long bones</div></li></ul><p>In older infants and children:</p><ul><li class="half_rhythm"><div>Developmental delays with or without hypotonia (Note: Intellect can be normal.)</div></li><li class="half_rhythm"><div>Failure to thrive</div></li><li class="half_rhythm"><div>Hearing loss</div></li><li class="half_rhythm"><div>Vision impairment</div></li><li class="half_rhythm"><div>Liver dysfunction</div></li><li class="half_rhythm"><div>Adrenal dysfunction</div></li><li class="half_rhythm"><div>Leukodystrophy</div></li><li class="half_rhythm"><div>Peripheral neuropathy and ataxia</div></li></ul></div><div id="pbd.Laboratory_Findings"><h4>Laboratory Findings</h4><p>The screening assays for ZSD are summarized in <a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object" rid-ob="figobpbdTscreeningassaysforzellwegerspe">Table 1</a>. Note that because some individuals with ZSD do not have abnormalities of these screening assays in body fluids or cultured cells, molecular genetic testing is necessary to establish the diagnosis (see <a href="#pbd.Establishing_the_Diagnosis">Establishing the Diagnosis</a>). Functional testing in fibroblasts remains an ancillary tool to confirm equivocal molecular and/or biochemical results.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTscreeningassaysforzellwegerspe"><a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object" title="Table 1. " class="img_link icnblk_img" rid-ob="figobpbdTscreeningassaysforzellwegerspe"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.screening_assays_for_zellweger_spe"><a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object" rid-ob="figobpbdTscreeningassaysforzellwegerspe">Table 1. </a></h4><p class="float-caption no_bottom_margin">Screening Assays for Zellweger Spectrum Disorder </p></div></div></div></div><div id="pbd.Establishing_the_Diagnosis"><h3>Establishing the Diagnosis</h3><p>The diagnosis of ZSD <b>is established</b> in a proband with the suggestive clinical and biochemical findings described in <a href="#pbd.Suggestive_Findings">Suggestive Findings</a> by identification of biallelic pathogenic (or likely pathogenic) variants in one of the 13 PEX genes listed in <a href="/books/NBK1448/table/pbd.T.molecular_genetic_testing_used_in/?report=objectonly" target="object" rid-ob="figobpbdTmoleculargenetictestingusedin">Table 2</a>.</p><dl class="temp-labeled-list"><dl class="bkr_refwrap"><dt>1.</dt><dd><p class="no_top_margin">One <i>PEX6</i> variant, <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Arg860Trp</a>, has been associated with ZSD in the heterozygous state due to allelic expression imbalance dependent on allelic background (see <a href="#pbd.Molecular_Genetics">Molecular Genetics</a>). (2) Per ACMG/AMP variant interpretation guidelines, the terms "pathogenic variants" and "likely pathogenic variants" are synonymous in a clinical setting, meaning that both are considered diagnostic and both can be used for clinical decision making [<a class="bibr" href="#pbd.REF.richards.2015.405" rid="pbd.REF.richards.2015.405">Richards et al 2015</a>]. Reference to "pathogenic variants" in this section is understood to include any likely pathogenic variants. (3) Identification of biallelic variants of uncertain significance (or of one known pathogenic variant and one variant of uncertain significance) in one of the 13 PEX genes listed in <a href="/books/NBK1448/table/pbd.T.molecular_genetic_testing_used_in/?report=objectonly" target="object" rid-ob="figobpbdTmoleculargenetictestingusedin">Table 2</a> does not establish or rule out the diagnosis.</p></dd></dl></dl><p>Molecular genetic testing approaches can include <b>gene-targeted testing</b> (multigene panel) and <b>comprehensive</b>
|
|
<b>genomic testing</b> (exome sequencing, genome sequencing), depending on the phenotype.</p><p>Gene-targeted testing requires that the clinician determine which gene(s) are likely involved, whereas genomic testing does not. Individuals with the suggestive clinical and biochemical findings of ZSD described in <a href="#pbd.Suggestive_Findings">Suggestive Findings</a> are likely to be diagnosed using gene-targeted testing (see <a href="#pbd.Option_1">Option 1</a>), whereas those with a nondistinct phenotype that does not suggest a specific diagnosis are more likely to be diagnosed using genomic testing (see <a href="#pbd.Option_2">Option 2</a>). Note: Single-gene testing (i.e., sequence analysis of one of the PEX genes, followed by gene-targeted deletion/duplication analysis) is rarely useful and typically NOT recommended. A multigene panel and/or exome sequencing are typically used in lieu of single-gene testing.</p><div id="pbd.Option_1"><h4>Option 1</h4><p><b>A multigene panel</b> for peroxisome biogenesis disorders that includes the 13 genes listed in <a href="/books/NBK1448/table/pbd.T.molecular_genetic_testing_used_in/?report=objectonly" target="object" rid-ob="figobpbdTmoleculargenetictestingusedin">Table 2</a> and other genes of interest (see <a href="#pbd.Differential_Diagnosis">Differential Diagnosis</a>) is most likely to identify the genetic cause of the condition while limiting identification of variants of uncertain significance and pathogenic variants in genes that do not explain the underlying phenotype.. Note: (1) The genes included in the panel and the diagnostic sensitivity of the testing used for each gene vary by laboratory and are likely to change over time. (2) Some multigene panels may include genes not associated with the condition discussed in this <i>GeneReview</i>. (3) In some laboratories, panel options may include a custom laboratory-designed panel and/or custom phenotype-focused exome analysis that includes genes specified by the clinician. (4) Methods used in a panel may include sequence analysis, deletion/duplication analysis, and/or other non-sequencing-based tests.</p><p>For an introduction to multigene panels click <a href="/books/n/gene/app5/?report=reader#app5.Multigene_Panels">here</a>. More detailed information for clinicians ordering genetic tests can be found <a href="/books/n/gene/app5/?report=reader#app5.Multigene_Panels_FAQs">here</a>.</p></div><div id="pbd.Option_2"><h4>Option 2</h4><p>When the clinical and laboratory findings in an affected individual do not lead to consideration of ZSD, <b>comprehensive genomic testing</b> (which does not require the clinician to determine which gene[s] are likely involved) can be the best option. <b>Exome sequencing</b> is most commonly used; <b>genome sequencing</b> is also possible.</p><p>For an introduction to comprehensive genomic testing click <a href="/books/n/gene/app5/?report=reader#app5.Comprehensive_Genomic_Testing">here</a>. More detailed information for clinicians ordering genomic testing can be found <a href="/books/n/gene/app5/?report=reader#app5.Comprehensive_Genomic_Testing_1">here</a>.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTmoleculargenetictestingusedin"><a href="/books/NBK1448/table/pbd.T.molecular_genetic_testing_used_in/?report=objectonly" target="object" title="Table 2. " class="img_link icnblk_img" rid-ob="figobpbdTmoleculargenetictestingusedin"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.molecular_genetic_testing_used_in"><a href="/books/NBK1448/table/pbd.T.molecular_genetic_testing_used_in/?report=objectonly" target="object" rid-ob="figobpbdTmoleculargenetictestingusedin">Table 2. </a></h4><p class="float-caption no_bottom_margin">Molecular Genetic Testing Used in Zellweger Spectrum Disorder (ZSD) </p></div></div></div></div></div><div id="pbd.Clinical_Characteristics"><h2 id="_pbd_Clinical_Characteristics_">Clinical Characteristics</h2><div id="pbd.Clinical_Description"><h3>Clinical Description</h3><p>Zellweger spectrum disorder (ZSD) is defined by a continuum of three phenotypes described before the biochemical and molecular bases of these disorders had been fully determined: Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD), and infantile <a href="/books/n/gene/refsum/?report=reader">Refsum disease</a> (IRD) [<a class="bibr" href="#pbd.REF.braverman.2016.313" rid="pbd.REF.braverman.2016.313">Braverman et al 2016</a>].</p><p>The ZSD phenotypic spectrum is broad; some affected individuals have mild manifestations, mainly sensory deficits and/or mild developmental delay. Recently, individuals with normal intellect have been identified [<a class="bibr" href="#pbd.REF.ratbi.2015.535" rid="pbd.REF.ratbi.2015.535">Ratbi et al 2015</a>, <a class="bibr" href="#pbd.REF.ratbi.2016.507" rid="pbd.REF.ratbi.2016.507">Ratbi et al 2016</a>, <a class="bibr" href="#pbd.REF.smith.2016.1565" rid="pbd.REF.smith.2016.1565">Smith et al 2016</a>] by genomic testing methods. Nonetheless, all of the peroxisome assembly disorders cause significant morbidity, frequently resulting in death in childhood.</p><p>Although the phenotypic designations listed above may be useful when evaluating undiagnosed individuals and counseling their families, one should not place too much emphasis on assigning a phenotypic label to an affected individual given that these phenotypes lie on a continuum. Thus, the terms "severe," "intermediate," and "milder" ZSD are now preferred. Because of the breadth of the phenotypic spectrum, individuals with ZSD mainly come to clinical attention in the newborn period or later in childhood. Occasionally, the subtlety of symptoms delays diagnosis until adulthood.</p><p><b>Newborns</b> are hypotonic with resultant poor feeding. Neonatal seizures are frequent and caused by underlying neuronal migration defects. Liver dysfunction may be evident as neonatal jaundice and elevation in liver function tests. Distinctive craniofacial features include flat face, broad nasal bridge, large anterior fontanelle, and widely split sutures. In severely affected children, bony stippling (chondrodysplasia punctata) at the patella(e) and the long bones may be noted, as well as renal cysts.</p><p><b>Older children</b> manifest retinal dystrophy, sensorineural hearing loss, developmental delay with hypotonia, and liver dysfunction. Children may first come to attention because of a failed hearing screen. Onset and severity of the hearing and visual problems vary. A few children with a clinical diagnosis of neonatal adrenoleukodystrophy had transient leopard spot pigmentary retinopathy [<a class="bibr" href="#pbd.REF.lyons.2004.191" rid="pbd.REF.lyons.2004.191">Lyons et al 2004</a>]. Liver dysfunction may be first identified in children with severe bleeding episodes caused by a vitamin K-responsive coagulopathy. Older children may develop adrenal insufficiency [<a class="bibr" href="#pbd.REF.berendse.2014.133" rid="pbd.REF.berendse.2014.133">Berendse et al 2014</a>] and osteopenia [<a class="bibr" href="#pbd.REF.rush.2016.33" rid="pbd.REF.rush.2016.33">Rush et al 2016</a>].</p><p><b>Adults</b> are rarely diagnosed with ZSD, but exceptions have been reported. Usually these are individuals with predominantly sensory deficits but normal neurologic development [<a class="bibr" href="#pbd.REF.moser.1995.13" rid="pbd.REF.moser.1995.13">Moser et al 1995</a>, <a class="bibr" href="#pbd.REF.raasrothschild.2002.1062" rid="pbd.REF.raasrothschild.2002.1062">Raas-Rothschild et al 2002</a>, <a class="bibr" href="#pbd.REF.majewski.2011.593" rid="pbd.REF.majewski.2011.593">Majewski et al 2011</a>, <a class="bibr" href="#pbd.REF.ratbi.2015.535" rid="pbd.REF.ratbi.2015.535">Ratbi et al 2015</a>, <a class="bibr" href="#pbd.REF.ratbi.2016.507" rid="pbd.REF.ratbi.2016.507">Ratbi et al 2016</a>, <a class="bibr" href="#pbd.REF.smith.2016.1565" rid="pbd.REF.smith.2016.1565">Smith et al 2016</a>].</p><div id="pbd.Severe_ZSD"><h4>Severe ZSD</h4><p>Severe ZSD (previously called Zellweger syndrome [ZS]) typically presents in the neonatal period with profound hypotonia, characteristic facies, gyral malformations, seizures, inability to feed, renal cysts, hepatic dysfunction, and chondrodysplasia punctata. Infants with severe ZSD are significantly impaired and usually die during the first year of life, usually having made no developmental progress. Death is usually secondary to progressive apnea or respiratory compromise from infection.</p></div><div id="pbd.IntermediateMilder_ZSD"><h4>Intermediate/Milder ZSD</h4><p>Intermediate/milder ZSD (previously called neonatal adrenoleukodystrophy [NALD] and infantile Refsum disease [IRD]) may present in the newborn period, but generally comes to attention later because of developmental delays, hearing loss, and/or visual impairment. Liver dysfunction may lead to a vitamin K-responsive coagulopathy. Children have also come to attention with episodes of hemorrhage; several children have presented in the first year of life with intracranial bleeding.</p><p>The clinical course is variable: while many children are very hypotonic, many learn to walk and talk.</p><p>Intermediate/milder ZSD is a progressive disorder with hearing and vision worsening with time. Some individuals may develop progressive degeneration of CNS myelin, a leukodystrophy, which may lead to loss of previously acquired skills and ultimately death.</p><p>Children who survive the first year and who have a non-progressive course have a 77% probability of reaching school age [<a class="bibr" href="#pbd.REF.pollthe.2004.333" rid="pbd.REF.pollthe.2004.333">Poll-The et al 2004</a>]. Some have normal intellect. They are at risk for adrenal insufficiency over time. Typically, they also have ameliogenesis imperfecta of the secondary teeth.</p></div><div id="pbd.Other"><h4>Other</h4><p>Individuals with atypical ZSD do not show sensory losses but have ataxia and peripheral neuropathy, and may have congenital cataracts (e.g., those with <i>PEX2</i>-ZSD [<a class="bibr" href="#pbd.REF.sevin.2011.8" rid="pbd.REF.sevin.2011.8">Sevin et al 2011</a>], <i>PEX11B-</i>ZSD [<a class="bibr" href="#pbd.REF.ebberink.2012.307" rid="pbd.REF.ebberink.2012.307">Ebberink et al 2012</a>], <i>PEX10</i>-ZSD [<a class="bibr" href="#pbd.REF.steinberg.2009.109" rid="pbd.REF.steinberg.2009.109">Steinberg et al 2009</a>], <i>PEX12</i>-ZSD [<a class="bibr" href="#pbd.REF.gootjes.2004.2077" rid="pbd.REF.gootjes.2004.2077">Gootjes et al 2004</a>], and <i>PEX16</i>-ZSD [<a class="bibr" href="#pbd.REF.ebberink.2010.608" rid="pbd.REF.ebberink.2010.608">Ebberink et al 2010</a>]).</p><p>Note that although Heimler syndrome [<a class="bibr" href="#pbd.REF.ratbi.2015.535" rid="pbd.REF.ratbi.2015.535">Ratbi et al 2015</a>, <a class="bibr" href="#pbd.REF.ratbi.2016.507" rid="pbd.REF.ratbi.2016.507">Ratbi et al 2016</a>, <a class="bibr" href="#pbd.REF.smith.2016.1565" rid="pbd.REF.smith.2016.1565">Smith et al 2016</a>] and ataxia (see <a class="bibr" href="#pbd.REF.r_gal.2010.259" rid="pbd.REF.r_gal.2010.259">Régal et al [2010]</a>, <a class="bibr" href="#pbd.REF.renaud.2016.1552" rid="pbd.REF.renaud.2016.1552">Renaud et al [2016]</a>) have been reported as unique phenotypes associated with PEX gene defects, the authors consider them part of the ZSD continuum. In general, screening assays of individuals described as having these milder phenotypes do not show the biochemical profile typical of ZSD (<a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object" rid-ob="figobpbdTscreeningassaysforzellwegerspe">Table 1</a>).</p></div><div id="pbd.Neuroimaging"><h4>Neuroimaging</h4><p>MRI may identify cortical gyral abnormalities and germinolytic cysts that are highly suggestive of severe ZSD. Other brain MRI findings have been identified over time in individuals with milder ZSD.</p><p>In a small number of individuals with ZSD, diffusion-weighted imaging and diffusion tensor imaging can be used to discern white matter damage not detected by standard imaging [<a class="bibr" href="#pbd.REF.patay.2005.2284" rid="pbd.REF.patay.2005.2284">Patay 2005</a>]. A demyelinating leukodystrophy can occur, but it is not clear which affected individuals are at increased risk for this development, or how it progresses in the individual.</p></div></div><div id="pbd.Phenotype_Correlations_by_Gene"><h3>Phenotype Correlations by Gene</h3><p>Biallelic pathogenic variants in the two most commonly involved genes, <i>PEX1</i> and <i>PEX6</i>, are associated with the full continuum of clinical phenotypes. This clinical variability, in general, is also found in individuals with biallelic pathogenic variants in <i>PEX10</i>, <i>PEX12</i>, and <i>PEX26</i>. Although in the past, defects in some of the less common PEX genes appeared to be associated with severe clinical phenotypes, more recently the phenotypic spectrum of defects in all PEX genes has been found to include both severely and mildly affected individuals. Overall clinical and biochemical severity appears to be most related to the genotype and not a particular PEX gene.</p></div><div id="pbd.GenotypePhenotype_Correlations"><h3>Genotype-Phenotype Correlations</h3><p>A general relationship appears to exist among the genotype, cellular phenotype (i.e., import of peroxisomal matrix proteins), and clinical phenotype [<a class="bibr" href="#pbd.REF.moser.1999.316" rid="pbd.REF.moser.1999.316">Moser 1999</a>]. PEX gene defects are associated with loss-of-function variants; hence, variants that abolish activity (e.g., large deletions, nonsense, frameshift variants) are most severe. In contrast, missense variants that retain some residual function have a less severe effect on peroxisome assembly; however, it should be noted that not all missense variants have residual activity.</p><p>Due to the overall rarity of ZSD the opportunities to rigorously assess genotype and phenotype are limited. The <i>PEX1</i> variants <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Ile700TyrfsTer42</a> and <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Gly843Asp</a> are exceptions, as hundreds of individuals homozygous or compound heterozygous for these variants have been identified (mostly in molecular research studies or clinical laboratories and not as part of a thorough natural history assessment).</p><ul><li class="half_rhythm"><div>Homozygosity for <i>PEX1</i>
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<a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Ile700TyrfsTer42</a> is associated with a more severe phenotype.</div></li><li class="half_rhythm"><div>Homozygosity for <i>PEX1</i>
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<a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Gly843Asp</a> has to date been associated with a milder ZSD phenotype and sometimes with an intermediate phenotype [<a class="bibr" href="#pbd.REF.pollthe.2004.333" rid="pbd.REF.pollthe.2004.333">Poll-The et al 2004</a>]. In addition, an adult with a normal neurologic examination and an ocular phenotype was reported [<a class="bibr" href="#pbd.REF.majewski.2011.593" rid="pbd.REF.majewski.2011.593">Majewski et al 2011</a>].</div></li></ul></div><div id="pbd.Nomenclature"><h3>Nomenclature</h3><p>Peroxisome biogenesis disorders (PBD) can be divided into two subtypes: the Zellweger spectrum disorder (ZSD) and the rhizomelic chondrodysplasia punctata spectrum, of which rhizomelic chondrodysplasia punctata type 1 (RCDP1) is one subtype. RCDP1 is caused by biallelic pathogenic variants in <i>PEX7</i>, the receptor that recognizes peroxisome enzymes containing peroxisomal targeting signal 2. While individuals with RCDP1 have a perturbation in matrix protein import consistent with a peroxisomal assembly defect, they have a biochemical, cellular, and clinical phenotype distinct from ZSD. (See <a href="/books/n/gene/rcdp/?report=reader">Rhizomelic Chondrodysplasia Punctata Type 1</a> for an in-depth description.)</p><p>ZSD has also formerly been referred to as cerebrohepatorenal syndrome, generalized peroxisomal disorders, Zellweger syndrome, neonatal adrenoleukodystrophy, or infantile Refsum disease (also known as infantile phytanic acid oxidase deficiency). Some individuals later shown to have ZSD were initially described as having hyperpipecolatemia or Heimler syndrome. The current preferred terminology is ZSD of severe, intermediate, or milder phenotype in order to recognize the common etiology, variations, and atypical presentations now being documented in individuals with biallelic pathogenic variants in any one of the 13 ZSD-PEX genes.</p><p>Of note, although Heimler syndrome [<a class="bibr" href="#pbd.REF.ratbi.2015.535" rid="pbd.REF.ratbi.2015.535">Ratbi et al 2015</a>, <a class="bibr" href="#pbd.REF.ratbi.2016.507" rid="pbd.REF.ratbi.2016.507">Ratbi et al 2016</a>, <a class="bibr" href="#pbd.REF.smith.2016.1565" rid="pbd.REF.smith.2016.1565">Smith et al 2016</a>] and ataxia (see <a class="bibr" href="#pbd.REF.r_gal.2010.259" rid="pbd.REF.r_gal.2010.259">Régal et al [2010]</a>, <a class="bibr" href="#pbd.REF.renaud.2016.1552" rid="pbd.REF.renaud.2016.1552">Renaud et al [2016]</a>) have been reported as unique phenotypes associated with PEX gene defects, the authors consider them part of the ZSD continuum.</p><p>Note: <a href="/books/n/gene/refsum/?report=reader">Refsum disease</a> is clinically and molecularly distinct from infantile Refsum disease.</p></div><div id="pbd.Prevalence"><h3>Prevalence</h3><p>ZSD occurs worldwide with varying prevalence. In the past the incidence of ZSD had been estimated at 1:50,000 [<a class="bibr" href="#pbd.REF.gould.2001" rid="pbd.REF.gould.2001">Gould et al 2001</a>]. More recent data from the New York state newborn screening laboratory confirmed 11 individuals with ZSD in more than 1.4 million screened for X-ALD using a biochemical assay (C26:0-LPC) that also detects ZSD (see <a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object" rid-ob="figobpbdTscreeningassaysforzellwegerspe">Table 1</a>) [<a class="bibr" href="#pbd.REF.hubbard.2006.185" rid="pbd.REF.hubbard.2006.185">Hubbard et al 2006</a>, <a class="bibr" href="#pbd.REF.hubbard.2009.212" rid="pbd.REF.hubbard.2009.212">Hubbard et al 2009</a>]. Thus, the confirmed incidence of ZSD in this population is 1:133,000 births [JJ Orsini, M Caggana, NY State Newborn Screening Laboratory Staff, personal communication, 2020]. Any estimate relying on a biochemical assay will be an underestimate because such assays fail to detect mild ZSD not associated with a definitive biochemical phenotype.</p><p>The main diagnostic center for peroxisomal diseases in Japan reported only 31 affected individuals over a 20-year period, with an estimated birth prevalence of 1:500,000 [<a class="bibr" href="#pbd.REF.shimozawa.2003.40" rid="pbd.REF.shimozawa.2003.40">Shimozawa et al 2003</a>]. This lower incidence in Japan is mainly due to the absence of the common European <i>PEX1</i> variants <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Ile700TyrfsTer42</a> and <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Gly843Asp</a>.</p></div></div><div id="pbd.Genetically_Related_Allelic_Disorder"><h2 id="_pbd_Genetically_Related_Allelic_Disorder_">Genetically Related (Allelic) Disorders</h2><p><i>PEX5</i> pathogenic variants in the alternate long form transcript (see <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_genesp/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordergenesp">Table 8</a>) that specifically affects the domain that binds to the PEX7 receptor are associated with rhizomelic chondrodysplasia punctata type 5 and not ZSD.</p><p>No phenotypes other than those discussed in this <i>GeneReview</i> have been associated with mutation of the other 12 ZSD-PEX genes (see <a href="/books/NBK1448/table/pbd.T.molecular_genetic_testing_used_in/?report=objectonly" target="object" rid-ob="figobpbdTmoleculargenetictestingusedin">Table 2</a>).</p></div><div id="pbd.Differential_Diagnosis"><h2 id="_pbd_Differential_Diagnosis_">Differential Diagnosis</h2><p>The differential diagnosis of Zellweger spectrum disorder (ZSD) varies with age at presentation and most prominent feature of the presentation. ZSD in newborns is most often confused with other conditions that result in profound hypotonia including Down syndrome, other chromosome abnormalities, and the disorders summarized in <a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd_in_a/?report=objectonly" target="object" rid-ob="figobpbdTdifferentialdiagnosisofzsdina">Table 3</a>.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTdifferentialdiagnosisofzsdina"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd_in_a/?report=objectonly" target="object" title="Table 3. " class="img_link icnblk_img" rid-ob="figobpbdTdifferentialdiagnosisofzsdina"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.differential_diagnosis_of_zsd_in_a"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd_in_a/?report=objectonly" target="object" rid-ob="figobpbdTdifferentialdiagnosisofzsdina">Table 3. </a></h4><p class="float-caption no_bottom_margin">Differential Diagnosis of ZSD in a Newborn with Profound Hypotonia </p></div></div><p>Approximately 15% of individuals with a ZSD-like clinical phenotype and increased plasma VLCFA concentration actually have a single-enzyme deficiency of peroxisomal β-oxidation (i.e., D-bifunctional enzyme deficiency or acyl-CoA oxidase deficiency) and do not have a pathogenic variant in a PEX gene. Therefore, in children with elevated plasma VLCFA but no additional biochemical evidence of ZSD, a broader peroxisomal multigene panel that includes at least <i>ACOX1</i> and <i>HSD17B4</i> in addition to the 13 PEX genes is recommended.</p><p>Other differential diagnoses of peroxisomal and non-peroxisomal disorders that do not necessarily present as profound neonatal hypotonia are summarized in <a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd__oth/?report=objectonly" target="object" rid-ob="figobpbdTdifferentialdiagnosisofzsdoth">Tables 4a</a> and <a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd__non/?report=objectonly" target="object" rid-ob="figobpbdTdifferentialdiagnosisofzsdnon">4b</a>, respectively.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTdifferentialdiagnosisofzsdoth"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd__oth/?report=objectonly" target="object" title="Table 4a. " class="img_link icnblk_img" rid-ob="figobpbdTdifferentialdiagnosisofzsdoth"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.differential_diagnosis_of_zsd__oth"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd__oth/?report=objectonly" target="object" rid-ob="figobpbdTdifferentialdiagnosisofzsdoth">Table 4a. </a></h4><p class="float-caption no_bottom_margin">Differential Diagnosis of ZSD – Other Peroxisomal Disorders </p></div></div><p><b>Contiguous <i>ABCD1</i>/DXS1375E deletion syndrome (CADDS).</b> An increase in plasma VLCFA concentration consistent with a defect in peroxisomal fatty acid metabolism can also be observed in CADDS, a contiguous deletion syndrome with a critical region spanning <i>ABCD1</i> and <i>BCAP31</i> [<a class="bibr" href="#pbd.REF.corzo.2002.1520" rid="pbd.REF.corzo.2002.1520">Corzo et al 2002</a>].</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTdifferentialdiagnosisofzsdnon"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd__non/?report=objectonly" target="object" title="Table 4b. " class="img_link icnblk_img" rid-ob="figobpbdTdifferentialdiagnosisofzsdnon"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.differential_diagnosis_of_zsd__non"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd__non/?report=objectonly" target="object" rid-ob="figobpbdTdifferentialdiagnosisofzsdnon">Table 4b. </a></h4><p class="float-caption no_bottom_margin">Differential Diagnosis of ZSD – Non-Peroxisomal Disorders </p></div></div></div><div id="pbd.Management"><h2 id="_pbd_Management_">Management</h2><p><a class="bibr" href="#pbd.REF.klouwer.2015.151" rid="pbd.REF.klouwer.2015.151">Klouwer et al [2015]</a> (<a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666198/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">full text</a>) and <a class="bibr" href="#pbd.REF.braverman.2016.313" rid="pbd.REF.braverman.2016.313">Braverman et al [2016]</a> (<a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214431/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">full text</a>) have published management and treatment guidelines for Zellweger spectrum disorder (ZSD).</p><div id="pbd.Evaluations_Following_Initial_Diagno"><h3>Evaluations Following Initial Diagnosis</h3><p>To establish the extent of disease and needs in an individual diagnosed with ZSD, the evaluations summarized in <a href="/books/NBK1448/table/pbd.T.recommended_evaluations_following/?report=objectonly" target="object" rid-ob="figobpbdTrecommendedevaluationsfollowing">Table 5</a> (if not performed as part of the evaluation that led to the diagnosis) are recommended.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTrecommendedevaluationsfollowing"><a href="/books/NBK1448/table/pbd.T.recommended_evaluations_following/?report=objectonly" target="object" title="Table 5. " class="img_link icnblk_img" rid-ob="figobpbdTrecommendedevaluationsfollowing"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.recommended_evaluations_following"><a href="/books/NBK1448/table/pbd.T.recommended_evaluations_following/?report=objectonly" target="object" rid-ob="figobpbdTrecommendedevaluationsfollowing">Table 5. </a></h4><p class="float-caption no_bottom_margin">Recommended Evaluations Following Initial Diagnosis in Individuals with Zellweger Spectrum Disorder </p></div></div></div><div id="pbd.Treatment_of_Manifestations"><h3>Treatment of Manifestations</h3><p>Treatment focuses on symptomatic therapy.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTtreatmentofmanifestationsinind"><a href="/books/NBK1448/table/pbd.T.treatment_of_manifestations_in_ind/?report=objectonly" target="object" title="Table 6. " class="img_link icnblk_img" rid-ob="figobpbdTtreatmentofmanifestationsinind"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.treatment_of_manifestations_in_ind"><a href="/books/NBK1448/table/pbd.T.treatment_of_manifestations_in_ind/?report=objectonly" target="object" rid-ob="figobpbdTtreatmentofmanifestationsinind">Table 6. </a></h4><p class="float-caption no_bottom_margin">Treatment of Manifestations in Individuals with Zellweger Spectrum Disorder </p></div></div></div><div id="pbd.Surveillance"><h3>Surveillance</h3><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTrecommendedsurveillanceforindiv"><a href="/books/NBK1448/table/pbd.T.recommended_surveillance_for_indiv/?report=objectonly" target="object" title="Table 7. " class="img_link icnblk_img" rid-ob="figobpbdTrecommendedsurveillanceforindiv"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.recommended_surveillance_for_indiv"><a href="/books/NBK1448/table/pbd.T.recommended_surveillance_for_indiv/?report=objectonly" target="object" rid-ob="figobpbdTrecommendedsurveillanceforindiv">Table 7. </a></h4><p class="float-caption no_bottom_margin">Recommended Surveillance for Individuals with Zellweger Spectrum Disorder </p></div></div></div><div id="pbd.Evaluation_of_Relatives_at_Risk"><h3>Evaluation of Relatives at Risk</h3><p>When the proband is on the milder end of the ZSD spectrum, it is appropriate to clarify the genetic status of apparently asymptomatic older and younger sibs in order to identify as early as possible those who are affected, and thus would benefit from annual hearing and ophthalmologic evaluation and routine monitoring of coagulation factors, adrenal function, and liver function. Note that molecular genetic testing for the pathogenic variants identified in the family is warranted as the results of screening assays (<a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object" rid-ob="figobpbdTscreeningassaysforzellwegerspe">Table 1</a>) in persons at the mild end of the ZSD spectrum may be highly variable.</p><p>See <a href="#pbd.Related_Genetic_Counseling_Issues"><u>Genetic Counseling</u></a> for issues related to testing of at-risk relatives for genetic counseling purposes.</p></div><div id="pbd.Therapies_Under_Investigation"><h3>Therapies Under Investigation</h3><p>Search <a href="https://clinicaltrials.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov</a> in the US and <a href="https://www.clinicaltrialsregister.eu/ctr-search/search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">EU Clinical Trials Register</a> in Europe for access to information on clinical studies for a wide range of diseases and conditions. Note: There may not be clinical trials for this disorder.</p></div></div><div id="pbd.Genetic_Counseling"><h2 id="_pbd_Genetic_Counseling_">Genetic Counseling</h2><p>
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<i>Genetic counseling is the process of providing individuals and families with
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information on the nature, mode(s) of inheritance, and implications of genetic disorders to help them
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make informed medical and personal decisions. The following section deals with genetic
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risk assessment and the use of family history and genetic testing to clarify genetic
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status for family members; it is not meant to address all personal, cultural, or
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ethical issues that may arise or to substitute for consultation with a genetics
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professional</i>. —ED.</p><div id="pbd.Mode_of_Inheritance"><h3>Mode of Inheritance</h3><p>Zellweger spectrum disorder (ZSD) is typically inherited in an autosomal recessive manner.</p><p>Note: One <i>PEX6</i> variant, <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Arg860Trp</a>, has been associated with ZSD in the heterozygous state due to allelic expression imbalance dependent on allelic background (see <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">Table 9</a>).</p></div><div id="pbd.Risk_to_Family_Members_Autosomal_Rec"><h3>Risk to Family Members (Autosomal Recessive Inheritance)</h3><p>
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<b>Parents of a proband</b>
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</p><ul><li class="half_rhythm"><div>The parents of an affected child are obligate heterozygotes (i.e., presumed to be carriers of one ZSD-causing pathogenic variant based on family history).</div></li><li class="half_rhythm"><div>Once the causative pathogenic variants have been identified in the proband, molecular genetic testing of the parents is recommended to confirm that both parents are heterozygous for a ZSD-causing pathogenic variant and to allow reliable recurrence risk assessment. (<i>De novo</i> variants are known to occur at a low but appreciable rate in autosomal recessive disorders [<a class="bibr" href="#pbd.REF.j_nsson.2017.519" rid="pbd.REF.j_nsson.2017.519">Jónsson et al 2017</a>].)</div></li><li class="half_rhythm"><div>Heterozygotes (carriers) are asymptomatic and are not at risk of developing the disorder.</div></li></ul><p>
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<b>Sibs of a proband</b>
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</p><ul><li class="half_rhythm"><div>If both parents are known to be heterozygous for a ZSD-causing pathogenic variant, each sib of an affected individual has at conception a 25% chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and not a carrier.</div></li><li class="half_rhythm"><div>In general, greater clinical variation is observed in families in which affected sibs are on the milder end of ZSD.</div></li><li class="half_rhythm"><div>Heterozygotes (carriers) are asymptomatic and are not at risk of developing the disorder.</div></li></ul><p>
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<b>Offspring of a proband</b>
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</p><ul><li class="half_rhythm"><div>In general, affected individuals do not reproduce.</div></li><li class="half_rhythm"><div>Some individuals with milder phenotypes may reproduce; the offspring of such individuals are obligate heterozygotes (carriers of a ZSD-causing pathogenic variant).</div></li></ul><p><b>Other family members.</b> Each sib of the proband's parents is at a 50% risk of being a carrier of a ZSD-causing pathogenic variant.</p><p>
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<b>Carrier detection</b>
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</p><ul><li class="half_rhythm"><div><b>Molecular genetic</b> carrier testing for at-risk relatives requires prior identification of the ZSD-causing pathogenic variants in the family.</div></li><li class="half_rhythm"><div><b>Biochemical</b> testing is not accurate for carrier testing, as the biochemical markers in carriers are normal.</div></li></ul></div><div id="pbd.Related_Genetic_Counseling_Issues"><h3>Related Genetic Counseling Issues</h3><p>See Management, <a href="#pbd.Evaluation_of_Relatives_at_Risk">Evaluation of Relatives at Risk</a> for information on evaluating at-risk relatives for the purpose of early diagnosis and treatment.</p><p>
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<b>Family planning</b>
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</p><ul><li class="half_rhythm"><div>The optimal time for determination of genetic risk, clarification of carrier status, and discussion of the availability of prenatal/preimplantation genetic testing is before pregnancy.</div></li><li class="half_rhythm"><div>It is appropriate to offer genetic counseling (including discussion of potential risks to offspring and reproductive options) to young adults who are affected, are carriers, or are at risk of being carriers.</div></li></ul><p><b>DNA banking.</b> Because it is likely that testing methodology and our understanding of genes, pathogenic mechanisms, and diseases will improve in the future, consideration should be given to banking DNA from probands in whom a molecular diagnosis has not been confirmed (i.e., the causative pathogenic mechanism is unknown). For more information, see <a class="bibr" href="#pbd.REF.huang.2022.389" rid="pbd.REF.huang.2022.389">Huang et al [2022]</a>.</p></div><div id="pbd.Prenatal_Testing_and_Preimplantation"><h3>Prenatal Testing and Preimplantation Genetic Testing</h3><p><b>Molecular genetic testing.</b> Once the ZSD-causing pathogenic variants have been identified in an affected family member, prenatal testing for a pregnancy at increased risk and preimplantation genetic testing for ZSD are possible.</p><p><b>Biochemical testing.</b> Biochemical testing using CVS or amniocytes may be used for prenatal diagnosis after confirming the biochemical defects in cultured fibroblasts from an affected family member. This approach may be helpful if DNA testing in the proband yields equivocal results or if DNA testing in the proband is not possible. (Note: Only a few specialized laboratories offer biochemical prenatal testing for ZSD.)</p><p>Biochemical testing of cultured amniocytes may also be useful when abnormalities suggestive of ZSD are detected on prenatal ultrasound examination.</p><p>Differences in perspective may exist among medical professionals and within families regarding the use of prenatal testing. While most centers would consider use of prenatal testing to be a personal decision, discussion of these issues may be helpful.</p></div></div><div id="pbd.Resources"><h2 id="_pbd_Resources_">Resources</h2><p>
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<i>GeneReviews staff has selected the following disease-specific and/or umbrella
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support organizations and/or registries for the benefit of individuals with this disorder
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and their families. GeneReviews is not responsible for the information provided by other
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organizations. For information on selection criteria, click <a href="/books/n/gene/app4/?report=reader">here</a>.</i></p>
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<ul><li class="half_rhythm"><div>
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<b>Global Foundation for Peroxisomal Disorders</b>
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</div><div>5147 South Harvard Avenue</div><div>Suite 181</div><div>Tulsa OK </div><div><b>Fax:</b> 918-516-0227</div><div><b>Email:</b> contactus@thegfpd.org</div><div>
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<a href="http://www.thegfpd.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">www.thegfpd.org</a>
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</div></li><li class="half_rhythm"><div>
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<b>National Institute of Neurological Disorders and Stroke (NINDS)</b>
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</div><div>PO Box 5801</div><div>Bethesda MD 20824</div><div><b>Phone:</b> 800-352-9424 (toll-free); 301-496-5751; 301-468-5981 (TTY)</div><div>
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<a href="https://www.ninds.nih.gov/Disorders/All-Disorders/Zellweger-Syndrome-Information-Page" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Zellweger Syndrome Information Page</a>
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</div></li><li class="half_rhythm"><div>
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<b>NCBI Genes and Disease</b>
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</div><div>
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<a href="/books/NBK22240/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Zellweger syndrome</a>
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</div></li><li class="half_rhythm"><div>
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<b>Newborn Screening in Your State</b>
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</div><div>Health Resources & Services Administration</div><div>
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<a href="https://newbornscreening.hrsa.gov/your-state" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">newbornscreening.hrsa.gov/your-state</a>
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</div></li><li class="half_rhythm"><div>
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<b>United Leukodystrophy Foundation</b>
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</div><div><b>Phone:</b> 815-748-0844</div><div><b>Email:</b> office@ulf.org</div><div>
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<a href="https://ulf.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ulf.org</a>
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</div></li></ul>
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</div><div id="pbd.Molecular_Genetics"><h2 id="_pbd_Molecular_Genetics_">Molecular Genetics</h2><p><i>Information in the Molecular Genetics and OMIM tables may differ from that elsewhere in the GeneReview: tables may contain more recent information. —</i>ED.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdmolgenTA"><a href="/books/NBK1448/table/pbd.molgen.TA/?report=objectonly" target="object" title="Table A." class="img_link icnblk_img" rid-ob="figobpbdmolgenTA"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.molgen.TA"><a href="/books/NBK1448/table/pbd.molgen.TA/?report=objectonly" target="object" rid-ob="figobpbdmolgenTA">Table A.</a></h4><p class="float-caption no_bottom_margin">Zellweger Spectrum Disorder: Genes and Databases </p></div></div><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdmolgenTB"><a href="/books/NBK1448/table/pbd.molgen.TB/?report=objectonly" target="object" title="Table B." class="img_link icnblk_img" rid-ob="figobpbdmolgenTB"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.molgen.TB"><a href="/books/NBK1448/table/pbd.molgen.TB/?report=objectonly" target="object" rid-ob="figobpbdmolgenTB">Table B.</a></h4><p class="float-caption no_bottom_margin">OMIM Entries for Zellweger Spectrum Disorder (View All in OMIM) </p></div></div><div id="pbd.Molecular_Pathogenesis"><h3>Molecular Pathogenesis</h3><p>Biallelic pathogenic variants in any one of the 13 PEX genes listed in <a href="/books/NBK1448/table/pbd.T.molecular_genetic_testing_used_in/?report=objectonly" target="object" rid-ob="figobpbdTmoleculargenetictestingusedin">Table 2</a> are known to cause Zellweger spectrum disorder (ZSD) in humans. These PEX genes encode proteins required for peroxisome biogenesis called "peroxins." Several peroxins are necessary for membrane biogenesis (PEX3, PEX16, and PEX19) and division (PEX11b), while the remaining genes associated with ZSD encode proteins comprising the peroxisomal matrix import machinery [<a class="bibr" href="#pbd.REF.waterham.2012.1430" rid="pbd.REF.waterham.2012.1430">Waterham & Ebberink 2012</a>, <a class="bibr" href="#pbd.REF.fujiki.2016.463" rid="pbd.REF.fujiki.2016.463">Fujiki 2016</a>].</p><p><b>Mechanism of disease causation</b>. PEX gene defects associated with ZSD reported to date are predicted to be loss-of-function variants.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTzellwegerspectrumdisordergenesp"><a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_genesp/?report=objectonly" target="object" title="Table 8. " class="img_link icnblk_img" rid-ob="figobpbdTzellwegerspectrumdisordergenesp"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.zellweger_spectrum_disorder_genesp"><a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_genesp/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordergenesp">Table 8. </a></h4><p class="float-caption no_bottom_margin">Zellweger Spectrum Disorder: Gene-Specific Laboratory Considerations </p></div></div><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figpbdTzellwegerspectrumdisordernotabl"><a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" title="Table 9. " class="img_link icnblk_img" rid-ob="figobpbdTzellwegerspectrumdisordernotabl"><img class="small-thumb" src="/corehtml/pmc/css/bookshelf/2.26/img/table-icon.gif" alt="Table Icon" /></a><div class="icnblk_cntnt"><h4 id="pbd.T.zellweger_spectrum_disorder_notabl"><a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">Table 9. </a></h4><p class="float-caption no_bottom_margin">Zellweger Spectrum Disorder: Notable Pathogenic Variants by Gene </p></div></div></div></div><div id="pbd.Chapter_Notes"><h2 id="_pbd_Chapter_Notes_">Chapter Notes</h2><div id="pbd.Author_History"><h3>Author History</h3><p>Nancy E Braverman, MS, MD (2003–present)<br />Ann B Moser, BA (2003–present)<br />Hugo W Moser, MD (2003–2007*)<br />Gerald V Raymond, MD (2003–present)<br />Steven J Steinberg, PhD (2003–present)</p><p>* Hugo W Moser, MD was Professor of Neurology and Pediatrics at Johns Hopkins University School of Medicine and former Director of the Kennedy Krieger Institute in Baltimore. He was a world-renowned expert in the field of neurogenetics. He was best known for his leadership role in understanding, diagnosing, and treating adrenoleukodystrophy (ALD). Dr Moser died of cancer on January 20, 2007 at age 82. He is greatly missed by his family, friends, colleagues, and patients.</p></div><div id="pbd.Revision_History"><h3>Revision History</h3><ul><li class="half_rhythm"><div>29 October 2020 (sw) Comprehensive update posted live</div></li><li class="half_rhythm"><div>21 December 2017 (sjs) Revision: <i>PEX6</i> pathogenic variant added</div></li><li class="half_rhythm"><div>16 November 2017 (bp) Comprehensive update posted live</div></li><li class="half_rhythm"><div>10 May 2012 (cd) Revision: to clarify that prenatal testing using biochemical methods is possible</div></li><li class="half_rhythm"><div>18 January 2011 (me) Comprehensive update posted live</div></li><li class="half_rhythm"><div>26 April 2006 (me) Comprehensive update posted live</div></li><li class="half_rhythm"><div>1 October 2004 (sjs) Revision</div></li><li class="half_rhythm"><div>12 December 2003 (me) Review posted live</div></li><li class="half_rhythm"><div>1 August 2003 (sjs) Original submission</div></li></ul></div></div><div id="pbd.References"><h2 id="_pbd_References_">References</h2><div id="pbd.Published_Guidelines__Consensus_Stat"><h3>Published Guidelines / Consensus Statements</h3><ul><li class="half_rhythm"><div>Braverman NE, Raymond GV , Rizzo WB, Moser AB, Wilkinson ME, Stone EM, Steinberg SJ, Wangler MF, Rush ET, Hacia JG, Bose M. Peroxisome biogenesis disorders in the Zellweger spectrum: an overview of current diagnosis, clinical manifestations, and treatment guidelines. Available <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214431/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">online</a>. 2016. Accessed 11-1-22.</div></li><li class="half_rhythm"><div>Klouwer FC, Berendse K, Ferdinandusse S, Wanders RJ, Engelen M, Poll-The BT. Zellweger spectrum disorders: clinical overview and management approach. Available <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666198/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">online</a>. 2015. Accessed 11-1-22.</div></li></ul></div><div id="pbd.Literature_Cited"><h3>Literature Cited</h3><ul class="simple-list"><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.abusafieh.2013.236">Abu-Safieh L, Alrashed M, Anazi S, Alkuraya H, Khan AO, Al-Owain M, Al-Zahrani J, Al-Abdi L, Hashem M, Al-Tarimi S, Sebai MA, Shamia A, Ray-Zack MD, Nassan M, Al-Hassnan ZN, Rahbeeni Z, Waheeb S, Alkharashi A, Abboud E, Al-Hazzaa SA, Alkuraya FS. Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes. <span><span class="ref-journal">Genome Res. </span>2013;<span class="ref-vol">23</span>:236–47.</span> [<a href="/pmc/articles/PMC3561865/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC3561865</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/23105016" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23105016</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.acharya.2012.112">Acharya BS, Ritwik P, Velasquez GM, Fenton SJ. Medical-dental findings and management of a child with infantile Refsum disease: a case report. <span><span class="ref-journal">Spec Care Dentist. </span>2012;<span class="ref-vol">32</span>:112–7.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/22591434" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 22591434</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.berendse.2014.133">Berendse K, Engelen M, Linthorst GE, van Trotsenburg AS, Poll-The BT. High prevalence of primary adrenal insufficiency in Zellweger spectrum disorders. <span><span class="ref-journal">Orphanet J Rare Dis. </span>2014;<span class="ref-vol">9</span>:133.</span> [<a href="/pmc/articles/PMC4164755/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4164755</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/25179809" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 25179809</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.berendse.2016.859">Berendse K, Klouwer FC, Koot BG, Kemper EM, Ferdinandusse S, Koelfat KV, Lenicek M, Schaap FG, Waterham HR, Vaz FM, Engelen M, Jansen PL, Wanders RJ, Poll-The BT. Cholic acid therapy in Zellweger spectrum disorders. <span><span class="ref-journal">J Inherit Metab Dis. </span>2016;<span class="ref-vol">39</span>:859–68.</span> [<a href="/pmc/articles/PMC5065608/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5065608</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/27469511" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 27469511</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.berendse.2019.955">Berendse K, Koot BGP, Klouwer FCC, Engelen M, Roels F, Lacle MM, Nikkels PGJ, Verheij J, Poll-The BT. Hepatic symptoms and histology in 13 patients with a Zellweger spectrum disorder. <span><span class="ref-journal">J Inherit Metab Dis. </span>2019;<span class="ref-vol">42</span>:955–65.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/31150129" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 31150129</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.braverman.2016.313">Braverman NE, Raymond GV, Rizzo WB, Moser AB, Wilkinson ME, Stone EM, Steinberg SJ, Wangler MF, Rush ET, Hacia JG, Bose M. Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines. <span><span class="ref-journal">Mol Genet Metab. </span>2016;<span class="ref-vol">117</span>:313–21.</span> [<a href="/pmc/articles/PMC5214431/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5214431</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/26750748" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26750748</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.collins.1999.45">Collins CS, Gould SJ. Identification of a common PEX1 mutation in Zellweger syndrome. <span><span class="ref-journal">Hum Mutat. </span>1999;<span class="ref-vol">14</span>:45–53.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/10447258" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 10447258</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.corzo.2002.1520">Corzo D, Gibson W, Johnson K, Mitchell G, LePage G, Cox GF, Casey R, Zeiss C, Tyson H, Cutting GR, Raymond GV, Smith KD, Watkins PA, Moser AB, Moser HW, Steinberg SJ. Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders. <span><span class="ref-journal">Am J Hum Genet. </span>2002;<span class="ref-vol">70</span>:1520–31.</span> [<a href="/pmc/articles/PMC419992/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC419992</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/11992258" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 11992258</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.ebberink.2010.608">Ebberink MS, Csanyi B, Chong WK, Denis S, Sharp P, Mooijer PA, Dekker CJ, Spooner C, Ngu LH, De Sousa C, Wanders RJ, Fietz MJ, Clayton PT, Waterham HR, Ferdinandusse S. Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene. <span><span class="ref-journal">J Med Genet. </span>2010;<span class="ref-vol">47</span>:608–15.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/20647552" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 20647552</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.ebberink.2012.307">Ebberink MS, Koster J, Visser G, Spronsen F, Stolte-Dijkstra I, Smit GP, Fock JM, Kemp S, Wanders RJ, Waterham HR. A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene. <span><span class="ref-journal">J Med Genet. </span>2012;<span class="ref-vol">49</span>:307–13.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/22581968" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 22581968</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.ebberink.2011.59">Ebberink MS, Mooijer PA, Gootjes J, Koster J, Wanders RJ, Waterham HR. Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder. <span><span class="ref-journal">Hum Mutat. </span>2011;<span class="ref-vol">32</span>:59–69.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/21031596" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21031596</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.ebberink.2009.93">Ebberink MS, Mooyer PA, Koster J, Dekker CJ, Eyskens FJ, Dionisi-Vici C, Clayton PT, Barth PG, Wanders RJ, Waterham HR. Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines. <span><span class="ref-journal">Hum Mutat. </span>2009;<span class="ref-vol">30</span>:93–8.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/18712838" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 18712838</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.falkenberg.2017.965">Falkenberg KD, Braverman NE, Moser AB, Steinberg SJ, Klouwer FCC, Schlüter A, Ruiz M, Pujol A, Engvall M, Naess K, van Spronsen F, Körver-Keularts I, Rubio-Gozalbo ME, Ferdinandusse S, Wanders RJA, Waterham HR. Allelic expression imbalance promoting a mutant PEX6 allele causes Zellweger spectrum disorder. <span><span class="ref-journal">Am J Hum Genet. </span>2017;<span class="ref-vol">101</span>:965–76.</span> [<a href="/pmc/articles/PMC5812895/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5812895</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/29220678" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 29220678</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.ferdinandusse.2017.330">Ferdinandusse S, Falkenberg KD, Koster J, Mooyer PA, Jones R, van Roermund CWT, Pizzino A, Schrader M, Wanders RJA, Vanderver A, Waterham HR. ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism. <span><span class="ref-journal">J Med Genet. </span>2017;<span class="ref-vol">54</span>:330–7.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/27799409" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 27799409</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.fujiki.2016.463">Fujiki Y. Peroxisome biogenesis and human peroxisome-deficiency disorders. <span><span class="ref-journal">Proc Jpn Acad Ser B Phys Biol Sci. </span>2016;<span class="ref-vol">92</span>:463–77.</span> [<a href="/pmc/articles/PMC5328784/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5328784</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/27941306" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 27941306</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.gootjes.2004.2077">Gootjes J, Skovby F, Christensen E, Wanders RJ, Ferdinandusse S. 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DNM1L-related mitochondrial fission defect presenting as refractory epilepsy. <span><span class="ref-journal">Eur J Hum Genet. </span>2016;<span class="ref-vol">24</span>:1084–8.</span> [<a href="/pmc/articles/PMC5070894/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5070894</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/26604000" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26604000</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.ventura.2016.75">Ventura MJ, Wheaton D, Xu M, Birch D, Bowne SJ, Sullivan LS, Daiger SP, Whitney AE, Jones RO, Moser AB, Chen R, Wangler MF. Diagnosis of a mild peroxisomal phenotype with next-generation sequencing. <span><span class="ref-journal">Mol Genet Metab Rep. </span>2016;<span class="ref-vol">9</span>:75–78.</span> [<a href="/pmc/articles/PMC5109284/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5109284</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/27872819" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 27872819</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.vogel.2015.599">Vogel BH, Bradley SE, Adams DJ, D'Aco K, Erbe RW, Fong C, Iglesias A, Kronn D, Levy P, Morrissey M, Orsini J, Parton P, Pellegrino J, Saavedra-Matiz CA, Shur N, Wasserstein M, Raymond GV, Caggana M. Newborn screening for X-linked adrenoleukodystrophy in New York State: diagnostic protocol, surveillance protocol and treatment guidelines. <span><span class="ref-journal">Mol Genet Metab. </span>2015;<span class="ref-vol">114</span>:599–603.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/25724074" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 25724074</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.waterham.2007.1736">Waterham HR, Koster J, van Roermund CWT, Mooyer PAW, Wanders RJA, Loenard JV. A lethal defect of mitochondrial and peroxisomal fission. <span><span class="ref-journal">N Engl J Med. </span>2007;<span class="ref-vol">356</span>:1736–41.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/17460227" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 17460227</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.waterham.2012.1430">Waterham HR, Ebberink MS. Genetics and molecular basis of human peroxisome biogenesis disorders. <span><span class="ref-journal">Biochim Biophys Acta. </span>2012;<span class="ref-vol">1822</span>:1430–41.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/22871920" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 22871920</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.watkins.1995.472">Watkins PA, McGuinness MC, Raymond GV, Hicks BA, Sisk JM, Moser AB, Moser HW. Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies. <span><span class="ref-journal">Ann Neurol. </span>1995;<span class="ref-vol">38</span>:472–7.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/7668838" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 7668838</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="pbd.REF.yoon.2016.313">Yoon G, Malam Z, Paton T, Marshall CR, Hyatt E, Ivakine Z, Scherer SW, Lee KS, Hawkins C, Cohn RD., Finding of Rare Disease Genes (FORGE) in Canada Consortium Steering Committee. Lethal disorder of mitochondrial fission caused by mutations in DNM1L. <span><span class="ref-journal">J Pediatr. </span>2016;<span class="ref-vol">171</span>:313–6.e1.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/26825290" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26825290</span></a>]</div></p></li></ul></div></div><div id="bk_toc_contnr"></div></div></div><div class="fm-sec"><h2 id="_NBK1448_pubdet_">Publication Details</h2><h3>Author Information and Affiliations</h3><div class="contrib half_rhythm"><span itemprop="author">Steven J Steinberg</span>, PhD<div class="affiliation small">ARUP Laboratories<br />Salt Lake City, Utah<div><span class="email-label">Email: </span><a href="mailto:dev@null" data-email="moc.balpura@grebniets.nevets" class="oemail">moc.balpura@grebniets.nevets</a></div></div></div><div class="contrib half_rhythm"><span itemprop="author">Gerald V Raymond</span>, MD<div class="affiliation small">Department of Genetic Medicine<br />Johns Hopkins Hospital<br />Baltimore, Maryland<div><span class="email-label">Email: </span><a href="mailto:dev@null" data-email="ude.imhj@4nomyarg" class="oemail">ude.imhj@4nomyarg</a></div></div></div><div class="contrib half_rhythm"><span itemprop="author">Nancy E Braverman</span>, MS, MD<div class="affiliation small">Departments of Pediatrics and Human Genetics<br />McGill University and Research Institute of the McGill University Health Center<br />Montreal, Quebec, Canada<div><span class="email-label">Email: </span><a href="mailto:dev@null" data-email="ac.lligcm@namrevarb.ycnan" class="oemail">ac.lligcm@namrevarb.ycnan</a></div></div></div><div class="contrib half_rhythm"><span itemprop="author">Ann B Moser</span>, BA<div class="affiliation small">The Peroxisomal Diseases Laboratory<br />Kennedy Krieger Institute<br />Department of Neurology<br />Johns Hopkins University School of Medicine<br />Baltimore, Maryland<div><span class="email-label">Email: </span><a href="mailto:dev@null" data-email="gro.regeirkydennek@aresom" class="oemail">gro.regeirkydennek@aresom</a></div></div></div><h3>Publication History</h3><p class="small">Initial Posting: <span itemprop="datePublished">December 12, 2003</span>; Last Update: <span itemprop="dateModified">October 29, 2020</span>.</p><h3>Copyright</h3><div><div class="half_rhythm"><a href="/books/about/copyright/">Copyright</a> © 1993-2025, University of Washington, Seattle. GeneReviews is
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contact: <a href="mailto:dev@null" data-email="ude.wu@tssamda" class="oemail">ude.wu@tssamda</a>.</p></div></div><h3>Publisher</h3><p><a href="http://www.washington.edu" ref="pagearea=page-banner&targetsite=external&targetcat=link&targettype=publisher">University of Washington, Seattle</a>, Seattle (WA)</p><h3>NLM Citation</h3><p>Steinberg SJ, Raymond GV, Braverman NE, et al. Zellweger Spectrum Disorder. 2003 Dec 12 [Updated 2020 Oct 29]. In: Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2025. <span class="bk_cite_avail"></span></p></div><div class="small-screen-prev"><a href="/books/n/gene/zap70-scid/?report=reader"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 100 100" preserveAspectRatio="none"><path d="M75,30 c-80,60 -80,0 0,60 c-30,-60 -30,0 0,-60"></path><text x="20" y="28" textLength="60" style="font-size:25px">Prev</text></svg></a></div><div class="small-screen-next"><a href="/books/n/gene/archived_chapters/?report=reader"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 100 100" preserveAspectRatio="none"><path d="M25,30c80,60 80,0 0,60 c30,-60 30,0 0,-60"></path><text x="20" y="28" textLength="60" style="font-size:25px">Next</text></svg></a></div></article><article data-type="table-wrap" id="figobpbdTc"><div id="pbd.Tc" class="table"><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.Tc/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.Tc_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.Tc_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">Zellweger Spectrum Disorder (ZSD): Included Phenotypes</th></tr></thead><tbody><tr><td headers="hd_h_pbd.Tc_1_1_1_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
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<ul><li class="half_rhythm"><div>Severe ZSD (previously called Zellweger syndrome)</div></li><li class="half_rhythm"><div>Intermediate/milder ZSD (previously called neonatal adrenoleukodystrophy, infantile Refsum disease, or Heimler syndrome)</div></li></ul>
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</td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin">For synonyms and outdated names see <a href="#pbd.Nomenclature"><u>Nomenclature</u></a>.</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTscreeningassaysforzellwegerspe"><div id="pbd.T.screening_assays_for_zellweger_spe" class="table"><h3><span class="label">Table 1. </span></h3><div class="caption"><p>Screening Assays for Zellweger Spectrum Disorder</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.screening_assays_for_zellweger_spe_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Compound</th><th id="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Test</th><th id="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Expected Findings</th><th id="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_4" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Limitations of Test</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">C26:0 LPC <sup>1</sup></td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Dried blood spot concentrations</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ C26:0-LPC concentrations</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Persons w/mild ZSD may not be detected.</td></tr><tr><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">VLCFA</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Plasma concentration</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ plasma concentrations of C26:0 & C26:1; ↑ ratios of C24/C22 & C26/C22 <sup>2</sup></td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Non-fasting samples, hemolyzed samples, or a person on a ketogenic diet can cause false positive results.</td></tr><tr><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Phytanic acid & pristanic acid <sup>3</sup></td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Plasma concentration</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ concentrations of phytanic acid &/or pristanic acid</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Branched-chain fatty acid accumulation depends on dietary intake of phytanic acid, which is minimal in formula- & breast-fed infants. Thus, phytanic & pristanic acid levels are normal in a neonate w/ZSD.</td></tr><tr><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Plasmalogens</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Erythrocyte membrane concentrations</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↓ amounts of C16 & C18 plasmalogens</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Persons w/moderate-to-mild ZSD may have marginally↓-to-normal plasmalogen levels.</td></tr><tr><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Pipecolic acid</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Plasma/urine concentration</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ concentration of pipecolic acid in both plasma & urine</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Urinary excretion of pipecolic acid is high in neonatal period but diminishes w/age. <sup>4</sup> Thus, urine should be tested in a neonate & plasma in an older child or adult.</td></tr><tr><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Bile acids</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Plasma/urine concentration</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ concentrations of C27 bile acid intermediates THCA & DHCA</td><td headers="hd_h_pbd.T.screening_assays_for_zellweger_spe_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">In most cases plasma testing is more sensitive than urine analysis.</td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin">DHCA = dihydroxycholestanoic acid; LPC = lysophosphatidylcholine; THCA = trihydroxycholestanoic acid; VLCFA = very-long-chain fatty acids</p></div></dd></dl><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.1.1"><p class="no_margin">C26:0-LPC is measured in dried blood spots (DBS) in newborn screening programs for <a href="/books/n/gene/x-ald/?report=reader">X-linked adrenoleukodystrophy</a> (X-ALD) in many states in the USA [<a class="bibr" href="#pbd.REF.vogel.2015.599" rid="pbd.REF.vogel.2015.599">Vogel et al 2015</a>, <a class="bibr" href="#pbd.REF.moser.2016.15" rid="pbd.REF.moser.2016.15">Moser et al 2016</a>]. Elevated C26:0-LPC concentrations are also detected in individuals with ZSD. Clinical evaluation, molecular testing, and additional biochemical testing of newborns with elevated C26:0-LPC on DBS can help to distinguish those with peroxisomal disorders other than X-ALD.</p></div></dd></dl><dl class="bkr_refwrap"><dt>2. </dt><dd><div id="pbd.TF.1.2"><p class="no_margin">Low plasma concentration of LDL and HDL can cause false negative results. In a person with low plasma concentrations of LDL and HDL without a defect in peroxisomal fatty acid metabolism, the plasma concentration of specific fatty acids (e.g., C22:0, C24:0, C26:0) are significantly lower than normal control levels. Persons with defects in peroxisomal fatty acid metabolism and very low LDL and HDL concentrations do not have significant elevations in C26:0 and C26:1, but do have modest elevations in the ratios of C24/C22 and C26/C22.</p></div></dd></dl><dl class="bkr_refwrap"><dt>3. </dt><dd><div id="pbd.TF.1.3"><p class="no_margin">This analysis is usually included in VLCFA measurement.</p></div></dd></dl><dl class="bkr_refwrap"><dt>4. </dt><dd><div id="pbd.TF.1.4"><p class="no_margin">Pipecolic acid measurement is an adjunct to more definitive biomarkers such as plasma VLCFA and erythrocyte plasmalogen levels. Elevations in pipecolic acid can also occur in <a href="/books/n/gene/pds/?report=reader">pyridoxine-dependent seizures</a> [<a class="bibr" href="#pbd.REF.plecko.2000.121" rid="pbd.REF.plecko.2000.121">Plecko et al 2000</a>].</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTmoleculargenetictestingusedin"><div id="pbd.T.molecular_genetic_testing_used_in" class="table"><h3><span class="label">Table 2. </span></h3><div class="caption"><p>Molecular Genetic Testing Used in Zellweger Spectrum Disorder (ZSD)</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.molecular_genetic_testing_used_in/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.molecular_genetic_testing_used_in_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" rowspan="2" scope="col" colspan="1" headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" style="text-align:left;vertical-align:middle;">Gene <sup>1, 2</sup></th><th id="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="2" scope="col" colspan="1" headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" style="text-align:left;vertical-align:middle;">% of ZSD Attributed to Pathogenic Variants in Gene <sup>3</sup></th><th id="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3" colspan="2" scope="colgroup" rowspan="1" style="text-align:left;vertical-align:middle;">Proportion of Pathogenic Variants <sup>4</sup> Detectable by Method</th></tr><tr><th headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3" id="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" colspan="1" scope="colgroup" rowspan="1" style="text-align:left;vertical-align:middle;">Sequence analysis <sup>5, 6</sup></th><th headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3" id="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Gene-targeted deletion/duplication analysis <sup>7</sup></th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>PEX1</i>
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</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">60.5%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">~98% <sup>8</sup></td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">~2% <sup>8</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>PEX6</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">14.5%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">77/77 <sup>9, 10</sup></td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_2" rowspan="12" colspan="1" style="text-align:left;vertical-align:middle;">Unknown <sup>11</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX12</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">7.6%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">43/43 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX26</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">4.2%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">17/17 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX10</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">3.4%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">17/18 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX2</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">3.1%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">19/22 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX5</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">2.0%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">13/13 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
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<i>PEX13</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">1.5%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">7/7 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
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<i>PEX16</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">1.1%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">8/8 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX3</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">0.7%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">3/3 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
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<i>PEX19</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">0.6%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">3/3 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
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<i>PEX14</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">0.5%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">1/2 <sup>9</sup></td></tr><tr><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
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<i>PEX11B</i>
|
|
</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">0.1%</td><td headers="hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_1_3 hd_h_pbd.T.molecular_genetic_testing_used_in_1_1_2_1" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">1/1 <sup>12</sup></td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.2.1"><p class="no_margin">Genes are listed from most frequent to least frequent genetic cause of ZSD.</p></div></dd></dl><dl class="bkr_refwrap"><dt>2. </dt><dd><div id="pbd.TF.2.2"><p class="no_margin">See <a href="/books/NBK1448/?report=reader#pbd.molgen.TA">Table A. Genes and Databases</a> for chromosome locus and protein.</p></div></dd></dl><dl class="bkr_refwrap"><dt>3. </dt><dd><div id="pbd.TF.2.3"><p class="no_margin">Based on complementation studies using somatic cell hybridization and/or cDNA complementation analysis in 810 individuals with biochemical confirmation of ZSD (197 at Kennedy Krieger Institute [unpublished] and 613 reported by <a class="bibr" href="#pbd.REF.ebberink.2011.59" rid="pbd.REF.ebberink.2011.59">Ebberink et al [2011]</a>)</p></div></dd></dl><dl class="bkr_refwrap"><dt>4. </dt><dd><div id="pbd.TF.2.4"><p class="no_margin">See <a href="#pbd.Molecular_Genetics">Molecular Genetics</a> for information on variants detected in these genes.</p></div></dd></dl><dl class="bkr_refwrap"><dt>5. </dt><dd><div id="pbd.TF.2.5"><p class="no_margin">Sequence analysis detects variants that are benign, likely benign, of uncertain significance, likely pathogenic, or pathogenic. Variants may include small intragenic deletions/insertions and missense, nonsense, and splice site variants; typically, exon or whole-gene deletions/duplications are not detected. For issues to consider in interpretation of sequence analysis results, click <a href="/books/n/gene/app2/?report=reader">here</a>.</p></div></dd></dl><dl class="bkr_refwrap"><dt>6. </dt><dd><div id="pbd.TF.2.6"><p class="no_margin">An estimate, based on the assumption that large deletions or promoter and deep intronic pathogenic variants would be missed; however, these types of variants do not appear to be common in ZSD.</p></div></dd></dl><dl class="bkr_refwrap"><dt>7. </dt><dd><div id="pbd.TF.2.7"><p class="no_margin">Gene-targeted deletion/duplication analysis detects intragenic deletions or duplications. Methods used may include a range of techniques such as quantitative PCR, long-range PCR, multiplex ligation-dependent probe amplification (MLPA), and a gene-targeted microarray designed to detect single-exon deletions or duplications.</p></div></dd></dl><dl class="bkr_refwrap"><dt>8. </dt><dd><div id="pbd.TF.2.8"><p class="no_margin">This estimate is based on the number of individuals identified with a <i>PEX1</i> defect, defined by having two pathogenic <i>PEX1</i> variants, one of which was a deletion detected by MLPA [Molly Sheridan, PhD; Johns Hopkins DNA Diagnostic Laboratory].</p></div></dd></dl><dl class="bkr_refwrap"><dt>9. </dt><dd><div id="pbd.TF.2.9"><p class="no_margin">Based on <a class="bibr" href="#pbd.REF.ebberink.2011.59" rid="pbd.REF.ebberink.2011.59">Ebberink et al [2011]</a>. The numerator is the number of individuals belonging to this complementation group who had two pathogenic variants identified and the denominator is the total number of individuals belonging to this complementation group who underwent sequencing of that gene.</p></div></dd></dl><dl class="bkr_refwrap"><dt>10. </dt><dd><div id="pbd.TF.2.10"><p class="no_margin">One <i>PEX6</i> variant, <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">p.Arg860Trp</a>, has been associated with ZSD in the heterozygous state due to allelic expression imbalance dependent on allelic background [<a class="bibr" href="#pbd.REF.falkenberg.2017.965" rid="pbd.REF.falkenberg.2017.965">Falkenberg et al [2017]</a>; see <a href="#pbd.Molecular_Genetics">Molecular Genetics</a>.</p></div></dd></dl><dl class="bkr_refwrap"><dt>11. </dt><dd><div id="pbd.TF.2.11"><p class="no_margin">No data on detection rate of gene-targeted deletion/duplication analysis are available.</p></div></dd></dl><dl class="bkr_refwrap"><dt>12. </dt><dd><div id="pbd.TF.2.12"><p class="no_margin"><i>PEX11B</i>: single case report [<a class="bibr" href="#pbd.REF.ebberink.2012.307" rid="pbd.REF.ebberink.2012.307">Ebberink et al 2012</a>]. <a class="bibr" href="#pbd.REF.taylor.2017.594" rid="pbd.REF.taylor.2017.594">Taylor et al [2017]</a> reported five additional individuals from three families. All had congenital cataracts and other clinical features, but normal or equivocal peroxisomal biomarkers in limited testing.</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTdifferentialdiagnosisofzsdina"><div id="pbd.T.differential_diagnosis_of_zsd_in_a" class="table"><h3><span class="label">Table 3. </span></h3><div class="caption"><p>Differential Diagnosis of ZSD in a Newborn with Profound Hypotonia</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd_in_a/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.differential_diagnosis_of_zsd_in_a_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Gene(s) / Genetic Mechanism</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Disorder</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">MOI</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>DMPK</i>
|
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Congenital <a href="/books/n/gene/myotonic-d/?report=reader">myotonic dystrophy type 1</a></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AD</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>MTM1</i>
|
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<a href="/books/n/gene/mtm/?report=reader">XL myotubular myopathy</a>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">XL</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">PWCR / imprinting defect</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<a href="/books/n/gene/pws/?report=reader">Prader-Willi syndrome</a>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">See footnote 1.</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>RYR1</i>
|
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<br />
|
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<i>SELENON</i>
|
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Multiminicore disease (OMIM <a href="https://www.omim.org/entry/255320" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">255320</a>, <a href="https://omim.org/entry/602771" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">602771</a>)</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>SMN1</i>
|
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<a href="/books/n/gene/sma/?report=reader">Spinal muscular atrophy</a>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd_in_a_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin">AD = autosomal dominant; AR = autosomal recessive; MOI = mode of inheritance; PWCR = Prader-Willi critical region; XL = X-linked</p></div></dd></dl><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.3.1"><p class="no_margin">The risk to the sibs of an affected child of having PWS depends on the genetic mechanism that resulted in the absence of expression of the paternally contributed 15q11.2-q13 region.</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTdifferentialdiagnosisofzsdoth"><div id="pbd.T.differential_diagnosis_of_zsd__oth" class="table"><h3><span class="label">Table 4a. </span></h3><div class="caption"><p>Differential Diagnosis of ZSD – Other Peroxisomal Disorders</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd__oth/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.differential_diagnosis_of_zsd__oth_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Gene</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Disorder</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">MOI</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_4" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Clinical Findings</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_5" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Biochemical Findings</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>ABCD1</i>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"><a href="/books/n/gene/x-ald/?report=reader">XL adrenoleukodystrophy</a> <sup>1</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">XL</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Affected males are almost always developmentally normal before initial presentation.</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ plasma VLCFA concentration in males; absence of other abnormalities of peroxisomes</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>ACBD5</i>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Retinal dystrophy w/leukodystrophy (OMIM <a href="https://omim.org/entry/618863" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">618863</a>) <sup>2</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">ZSD-like clinical phenotype</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ plasma VLCFA concentration, mild ↓ in plasmalogens</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>ACOX1</i>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Acyl-CoA oxidase deficiency (OMIM <a href="https://omim.org/entry/264470" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">264470</a>) <sup>3</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Intermediate ZSD-like clinical phenotype</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ plasma VLCFA concentration <sup>3</sup></td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>DNM1L</i>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Lethal encephalopathy due to defective mitochondrial peroxisomal fission 1 <sup>4</sup> (OMIM <a href="https://omim.org/entry/614388" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">614388</a>)</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AD<br />AR</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Mildly dysmorphic facial features, truncal hypotonia, absent tendon reflexes, microcephaly, optic atrophy, failure to thrive, & severe DD</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Mildly ↑ plasma VLCFA & persistent lactic acidemia</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>HSD17B4</i>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">D-bifunctional enzyme deficiency (OMIM <a href="https://omim.org/entry/261515" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">261515</a>) <sup>2</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Spectrum of severity: from severe ZSD-like clinical phenotype (often presents w/severe seizures) to milder presentations w/normal biochemistry <sup>5</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ plasma VLCFA concentration, branched chain fatty acids (pristanic & phytanic acids) & ↑ bile acid intermediates (THCA/DHCA)</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>SCP2</i>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Leukoencephalopathy w/dystonia & motor neuropathy (OMIM <a href="https://omim.org/entry/613724" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">613724</a>) <sup>2</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">ZSD-like clinical phenotype</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__oth_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">↑ plasma VLCFA concentration</td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin">AD = autosomal dominant; AR = autosomal recessive; DD = developmental delay; DHCA = dihydroxycholestanoic acid; Mat = maternal; MOI = mode of inheritance; SNHL = sensorineural hearing loss; THCA = trihydroxycholestanoic acid; VLCFA = very-long-chain fatty acid; XL = X-linked; ZSD = Zellweger spectrum disorder</p></div></dd></dl><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.4a.1"><p class="no_margin">See <a class="bibr" href="#pbd.REF.tran.2014.262" rid="pbd.REF.tran.2014.262">Tran et al [2014]</a> for an example of a <i>PEX6</i> defect mistaken for X-linked adrenoleukodystrophy.</p></div></dd></dl><dl class="bkr_refwrap"><dt>2. </dt><dd><div id="pbd.TF.4a.2"><p class="no_margin"><a class="bibr" href="#pbd.REF.abusafieh.2013.236" rid="pbd.REF.abusafieh.2013.236">Abu-Safieh et al [2013]</a>, <a class="bibr" href="#pbd.REF.ferdinandusse.2017.330" rid="pbd.REF.ferdinandusse.2017.330">Ferdinandusse et al [2017]</a></p></div></dd></dl><dl class="bkr_refwrap"><dt>3. </dt><dd><div id="pbd.TF.4a.3"><p class="no_margin">See <a class="bibr" href="#pbd.REF.watkins.1995.472" rid="pbd.REF.watkins.1995.472">Watkins et al [1995]</a> for a comparison of acyl-CoA oxidase deficiency and ZSD.</p></div></dd></dl><dl class="bkr_refwrap"><dt>4. </dt><dd><div id="pbd.TF.4a.4"><p class="no_margin"><a class="bibr" href="#pbd.REF.waterham.2007.1736" rid="pbd.REF.waterham.2007.1736">Waterham et al [2007]</a>, <a class="bibr" href="#pbd.REF.sheffer.2016.1603" rid="pbd.REF.sheffer.2016.1603">Sheffer et al [2016]</a>, <a class="bibr" href="#pbd.REF.vanstone.2016.1084" rid="pbd.REF.vanstone.2016.1084">Vanstone et al [2016]</a>, <a class="bibr" href="#pbd.REF.yoon.2016.313" rid="pbd.REF.yoon.2016.313">Yoon et al [2016]</a></p></div></dd></dl><dl class="bkr_refwrap"><dt>5. </dt><dd><div id="pbd.TF.4a.5"><p class="no_margin"><a class="bibr" href="#pbd.REF.pierce.2010.282" rid="pbd.REF.pierce.2010.282">Pierce et al [2010]</a>, <a class="bibr" href="#pbd.REF.lines.2014.963" rid="pbd.REF.lines.2014.963">Lines et al [2014]</a></p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTdifferentialdiagnosisofzsdnon"><div id="pbd.T.differential_diagnosis_of_zsd__non" class="table"><h3><span class="label">Table 4b. </span></h3><div class="caption"><p>Differential Diagnosis of ZSD – Non-Peroxisomal Disorders</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.differential_diagnosis_of_zsd__non/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.differential_diagnosis_of_zsd__non_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Gene(s)</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Disorder / Phenotype</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">MOI</th><th id="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_4" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Clinical Findings</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">>100 genes <sup>1</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<a href="/books/n/gene/deafness-overview/?report=reader">Hereditary hearing loss & deafness</a>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AD<br />AR<br />XL<br />Mat</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">SNHL</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">>24 genes <sup>2</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<a href="/books/n/gene/lca-ov/?report=reader">Leber congenital amaurosis / early-onset severe retinal dystrophy</a>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR<br />(AD)</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Progressive visual loss</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">~350 genes <sup>3</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<a href="/books/n/gene/mt-overview/?report=reader">Mitochondrial disease</a>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR<br />AD<br />Mat</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">May only affect a single organ or may involve multiple organ systems; often presents w/prominent neurologic & myopathic features</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">>80 genes <sup>4</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<a href="/books/n/gene/rp-overview/?report=reader">Retinitis pigmentosa</a>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AD<br />AR<br />XL<br />(Digenic)</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Progressive visual loss</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>ADGRV1</i>
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<br />
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<i>CDH23</i>
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<br />
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<i>CIB2</i>
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<br />
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<i>MYO7A</i>
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<br />
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<i>PCDH15</i>
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<br />
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<i>USH1C</i>
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<br />
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<i>USH1G</i>
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<br />
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<i>USH1H</i>
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<br />
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<i>USH2A</i>
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<br />
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<i>WHRN</i>
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</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"><a href="/books/n/gene/usher1/?report=reader">Usher syndrome type I</a> & <a href="/books/n/gene/usher2/?report=reader">type II</a></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AR</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<ul><li class="half_rhythm"><div>Type 1: Congenital, bilateral, profound SNHL, vestibular areflexia, & RP</div></li><li class="half_rhythm"><div>Type 2: Congenital, bilateral SNHL & RP</div></li></ul>
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</td></tr><tr><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">>100 genes</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Hereditary leukodystrophies <sup>5</sup></td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">AD<br />AR<br />XL<br />Mat</td><td headers="hd_h_pbd.T.differential_diagnosis_of_zsd__non_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Progressive spasticity w/loss of previous skills</td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin">AD = autosomal dominant; AR = autosomal recessive; Mat = maternal; MOI = mode of inheritance; RP = retinitis pigmentosa; SNHL = sensorineural hearing loss; XL = X-linked</p></div></dd></dl><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.4b.1"><p class="no_margin">See <a href="/books/n/gene/deafness-overview/?report=reader">Hereditary Hearing Loss and Deafness Overview</a>.</p></div></dd></dl><dl class="bkr_refwrap"><dt>2. </dt><dd><div id="pbd.TF.4b.2"><p class="no_margin">See <a href="/books/n/gene/lca-ov/?report=reader">Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy Overview</a>.</p></div></dd></dl><dl class="bkr_refwrap"><dt>3. </dt><dd><div id="pbd.TF.4b.3"><p class="no_margin">See <a href="/books/n/gene/mt-overview/?report=reader">Mitochondrial Disease Overview</a>.</p></div></dd></dl><dl class="bkr_refwrap"><dt>4. </dt><dd><div id="pbd.TF.4b.4"><p class="no_margin">See <a href="/books/n/gene/rp-overview/?report=reader">Retinitis Pigmentosa Overview</a>.</p></div></dd></dl><dl class="bkr_refwrap"><dt>5. </dt><dd><div id="pbd.TF.4b.5"><p class="no_margin">See <a class="bibr" href="#pbd.REF.parikh.2015.501" rid="pbd.REF.parikh.2015.501">Parikh et al [2015]</a>, Table 2: Major neurologic signs and symptoms in the leukodystrophies.</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTrecommendedevaluationsfollowing"><div id="pbd.T.recommended_evaluations_following" class="table"><h3><span class="label">Table 5. </span></h3><div class="caption"><p>Recommended Evaluations Following Initial Diagnosis in Individuals with Zellweger Spectrum Disorder</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.recommended_evaluations_following/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.recommended_evaluations_following_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">System/Concern</th><th id="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Evaluation</th><th id="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Comment</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Gastrointestinal/</b>
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<br />
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<b>Feeding</b>
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</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Feeding & nutrition assessment</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<ul><li class="half_rhythm"><div>To incl eval of aspiration risk & nutritional status</div></li><li class="half_rhythm"><div>Consider eval for gastric tube placement in those w/dysphagia &/or aspiration risk.</div></li></ul>
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</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Hearing</b>
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</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Audiologic eval</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Assess for hearing loss.</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Eyes</b>
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</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Comprehensive ophthalmologic assessment</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">OCT exam in compliant patients has shown cystoid macular edema [<a class="bibr" href="#pbd.REF.ventura.2016.75" rid="pbd.REF.ventura.2016.75">Ventura et al 2016</a>].</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
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<b>Hepatic</b>
|
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</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<ul><li class="half_rhythm"><div>Liver function testing (AST, ALT, total & direct bilirubin, PT, PTT, INR)</div></li><li class="half_rhythm"><div>C27 bile acid intermediates (DHCA & THCA)</div></li><li class="half_rhythm"><div>Ultrasound eval &/or liver fibroscan</div></li></ul>
|
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</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Liver fibrosis can occur insidiously over time; portal hypertension & esophageal varices can occur; rare adults have developed hepatocellular carcinoma in the setting of fibrosis [<a class="bibr" href="#pbd.REF.berendse.2019.955" rid="pbd.REF.berendse.2019.955">Berendse et al 2019</a>, <a class="bibr" href="#pbd.REF.heubi.2018.661" rid="pbd.REF.heubi.2018.661">Heubi & Bishop 2018</a>].</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Neurologic</b>
|
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</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Neurologic eval</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<ul><li class="half_rhythm"><div>To incl brain MRI</div></li><li class="half_rhythm"><div>Consider EEG if seizures are a concern.</div></li></ul>
|
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</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Development</b>
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</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Developmental assessment</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<ul><li class="half_rhythm"><div>To incl motor, adaptive, cognitive, & speech/language eval</div></li><li class="half_rhythm"><div>Eval for early intervention / special education</div></li></ul>
|
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</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" rowspan="2" scope="row" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Endocrine</b>
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</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<ul><li class="half_rhythm"><div>Eval of adrenal function (ACTH & cortisol)</div></li><li class="half_rhythm"><div>Consideration of ACTH stimulation test as appropriate</div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Adrenal insufficiency may occur during periods of stress.</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" colspan="1" scope="row" rowspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Eval of bone density by DXA</div></li><li class="half_rhythm"><div>Consider serum vitamin D level.</div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Pathologic fractures have occurred in persons at all ages; evaluate as clinically indicated [<a class="bibr" href="#pbd.REF.rush.2016.33" rid="pbd.REF.rush.2016.33">Rush et al 2016</a>].</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Renal</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Urine oxalate /creatinine ratio, serial renal ultrasound (can be done w/liver ultrasounds)</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Some patients develop urolithiasis & nephrocalcinosis assoc w/urinary oxalate load [<a class="bibr" href="#pbd.REF.van_woerden.2006.346" rid="pbd.REF.van_woerden.2006.346">van Woerden et al 2006</a>].</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Dental</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Dental eval</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Ameliogenesis imperfects, typically of secondary teeth, requires extensive dental interventions.</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Genetic</b>
|
|
<br />
|
|
<b>counseling</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">By genetics professionals <sup>1</sup></td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">To inform patients & families re nature, MOI, & implications of ZSD in order to facilitate medical & personal decision making</td></tr><tr><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Family support</b>
|
|
<br />
|
|
<b>& resources</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Assess need for:
|
|
<ul><li class="half_rhythm"><div>Community or <a href="#pbd.Resources">online resources</a> such as <a href="https://www.p2pusa.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Parent to Parent</a>;</div></li><li class="half_rhythm"><div>Social work involvement for parental support;</div></li><li class="half_rhythm"><div>Home nursing referral.</div></li></ul></td><td headers="hd_h_pbd.T.recommended_evaluations_following_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"></td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin">DHCA = dihydroxycholestanoic acid; DXA = dual-energy x-ray absorptiometry; MOI = mode of inheritance; OCT = optical coherence tomography; THCA = trihydroxycholestanoic acid</p></div></dd></dl><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.5.1"><p class="no_margin">Medical geneticist, certified genetic counselor, certified advanced genetic nurse</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTtreatmentofmanifestationsinind"><div id="pbd.T.treatment_of_manifestations_in_ind" class="table"><h3><span class="label">Table 6. </span></h3><div class="caption"><p>Treatment of Manifestations in Individuals with Zellweger Spectrum Disorder</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.treatment_of_manifestations_in_ind/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.treatment_of_manifestations_in_ind_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Manifestation/<br />Concern</th><th id="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Treatment</th><th id="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Considerations/Other</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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|
<b>Feeding &</b>
|
|
<br />
|
|
<b>nutrition</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Feeding therapy; gastrostomy tube placement may be required for persistent feeding issues.</div></li><li class="half_rhythm"><div>No specific metabolic diet recommended <sup>1</sup></div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">W/many children having some degree of malabsorption, elemental formulas may be better tolerated.</td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Hearing</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Hearing aids in children found to have hearing impairment</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">See also <a href="/books/n/gene/deafness-overview/?report=reader">Hereditary Hearing Loss and Deafness Overview</a> for discussion of management issues.</td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Vision</b>
|
|
<br />
|
|
<b>impairment</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Cataract removal to preserve vision</div></li><li class="half_rhythm"><div>Glasses to correct refractive errors</div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"></td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Liver</b>
|
|
<br />
|
|
<b>dysfunction</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Supplementation of vitamin K & other fat-soluble vitamins</div></li><li class="half_rhythm"><div>Cholbam<sup>TM</sup> (cholic acid) supplementation <sup>2</sup></div></li><li class="half_rhythm"><div>Varices can be treated w/sclerosing therapies.</div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Cholic acid supplementation can worsen liver disease in individuals with preexisting fibrosis & advanced liver disease [<a class="bibr" href="#pbd.REF.berendse.2016.859" rid="pbd.REF.berendse.2016.859">Berendse et al 2016</a>].</td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Seizures</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Standard treatment w/ASM by experienced neurologist</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">No type of ASM is contraindicated. Seizures may be difficult to control despite use of appropriate medication.</td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>DD/ID</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Provide early-intervention services.</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"></td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Adrenal</b>
|
|
<br />
|
|
<b>insufficiency</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Adrenal replacement therapy</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"></td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Osteopenia</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Vitamin D supplementation</div></li><li class="half_rhythm"><div>Consider bisphosphonate.</div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Benefits of bisphosphonate treatment noted in 1 case report [<a class="bibr" href="#pbd.REF.rush.2016.33" rid="pbd.REF.rush.2016.33">Rush et al 2016</a>]</td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Ameliogenesis</b>
|
|
<br />
|
|
<b>imperfecta</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Treatment per dentist</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"><a class="bibr" href="#pbd.REF.tran.2011.266" rid="pbd.REF.tran.2011.266">Tran et al [2011]</a>, <a class="bibr" href="#pbd.REF.acharya.2012.112" rid="pbd.REF.acharya.2012.112">Acharya et al [2012]</a></td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Renal oxalate</b>
|
|
<br />
|
|
<b>stones</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Supportive treatment has included hydration, lithotripsy, surgical intervention.</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Pyridoxine treatment did not ↓ oxalate excretion in 1 study [<a class="bibr" href="#pbd.REF.van_woerden.2006.346" rid="pbd.REF.van_woerden.2006.346">van Woerden et al 2006</a>].</td></tr><tr><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Vaccination</b>
|
|
</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Annual influenza & respiratory syncytial virus vaccines as well as usual vaccination schedule</td><td headers="hd_h_pbd.T.treatment_of_manifestations_in_ind_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"></td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin">ASM = anti-seizure medication; DD = developmental delay; ID = intellectual disability</p></div></dd></dl><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.6.1"><p class="no_margin">A diet low in phytanic acid has been proposed, based mainly on the weak analogy with adult <a href="/books/n/gene/refsum/?report=reader">Refsum disease</a>, in which accumulation of phytanic acid is pathogenic and treatment involves restricted dietary intake of phytanic acid (including avoidance of full-fat cow's milk products and high-fat meat products from ruminants). Its effectiveness in ZSD has never been proven. All standard infant formulas are already low in phytanic acid.</p></div></dd></dl><dl class="bkr_refwrap"><dt>2. </dt><dd><div id="pbd.TF.6.2"><p class="no_margin">By providing the final C24 bile acid product, the bile acid pathway undergoes feedback inhibition, thus reducing the levels of elevated C27 bile acid intermediates that are thought to be toxic to the liver. Cholic acid therapy does in fact decrease C27 bile acid intermediates (which should be measured), but its clinical effect in ZSD is not yet known.</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTrecommendedsurveillanceforindiv"><div id="pbd.T.recommended_surveillance_for_indiv" class="table"><h3><span class="label">Table 7. </span></h3><div class="caption"><p>Recommended Surveillance for Individuals with Zellweger Spectrum Disorder</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.recommended_surveillance_for_indiv/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.recommended_surveillance_for_indiv_lrgtbl__"><table><thead><tr><th id="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">System/Concern</th><th id="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Evaluation</th><th id="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Frequency</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Feeding</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Measurement of growth parameters</div></li><li class="half_rhythm"><div>Eval of nutritional status & safety of oral intake</div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">At each visit</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Hearing</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Audiology eval</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="2" colspan="1" style="text-align:left;vertical-align:middle;">Annually</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Eyes</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Ophthalmologic eval</div></li><li class="half_rhythm"><div>Visual field testing</div></li></ul>
|
|
</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Hepatic</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Coagulation factors & other synthetic liver functions (PT, PTT, AST, ALT, total & direct bilirubin)</div></li><li class="half_rhythm"><div>Ultrasound &/or fibroscan to evaluate liver architecture</div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Annually; persons w/overt hepatic dysfunction require more frequent monitoring.</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" rowspan="2" scope="row" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Neurologic</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Monitor those w/seizures as clinically indicated.</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">At each visit</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" colspan="1" scope="row" rowspan="1" style="text-align:left;vertical-align:middle;">Head MRI to evaluate for white matter changes that may explain changes in cognitive &/or motor ability</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">As needed</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Development</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Monitor developmental progress & educational needs.</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">At each visit</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Endocrine</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Assess adrenal function (ACTH & cortisol).</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">By age 1 yr; annually thereafter</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Dental</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Dental exam</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Every 6 mos after dental eruption</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Renal stones</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<ul><li class="half_rhythm"><div>Urine oxalate-to-creatinine ratio</div></li><li class="half_rhythm"><div>Consider renal imaging when performing liver imaging.</div></li></ul>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Annually</td></tr><tr><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<b>Miscellaneous/</b>
|
|
<br />
|
|
<b>Other</b>
|
|
</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">Assess family need for social work support (e.g., palliative/respite care, home nursing, other local resources) & care coordination.</td><td headers="hd_h_pbd.T.recommended_surveillance_for_indiv_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">At each visit</td></tr></tbody></table></div></div></article><article data-type="table-wrap" id="figobpbdmolgenTA"><div id="pbd.molgen.TA" class="table"><h3><span class="label">Table A.</span></h3><div class="caption"><p>Zellweger Spectrum Disorder: Genes and Databases</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.molgen.TA/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.molgen.TA_lrgtbl__"><table class="no_bottom_margin"><tbody><tr><th id="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">Gene</th><th id="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">Chromosome Locus</th><th id="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">Protein</th><th id="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">Locus-Specific Databases</th><th id="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">HGMD</th><th id="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">ClinVar</th></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5189" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX1</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5189" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">7q21<wbr style="display:inline-block"></wbr>​.2</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/O43933" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal ATPase PEX1</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX1 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX1 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX1</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX1[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX1</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5828" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX2</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5828" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">8q21<wbr style="display:inline-block"></wbr>​.13</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/P28328" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisome biogenesis factor 2</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX2" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX2 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX2" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX2 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX2" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX2</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX2[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX2</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/8504" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX3</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=8504" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">6q24<wbr style="display:inline-block"></wbr>​.2</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/P56589" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal biogenesis factor 3</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX3" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX3 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX3" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX3 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX3" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX3</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX3[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX3</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5830" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX5</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5830" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">12p13<wbr style="display:inline-block"></wbr>​.31</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/P50542" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal targeting signal 1 receptor</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX5" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX5 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX5" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX5 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX5" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX5</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX5[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX5</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5190" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX6</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5190" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">6p21<wbr style="display:inline-block"></wbr>​.1</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/Q13608" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal ATPase PEX6</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX6" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX6 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX6" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX6 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX6" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX6</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX6[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX6</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5192" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX10</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5192" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">1p36<wbr style="display:inline-block"></wbr>​.32</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/O60683" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisome biogenesis factor 10</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX10" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX10 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX10" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX10 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX10" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX10</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX10[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX10</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/8799" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX11B</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=8799" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">1q21<wbr style="display:inline-block"></wbr>​.1</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/O96011" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal membrane protein 11B</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;"></td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX11B" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX11B</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX11B[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX11B</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5193" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX12</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5193" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">17q12</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/O00623" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisome assembly protein 12</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX12" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX12 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX12" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX12 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX12" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX12</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX12[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX12</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5194" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX13</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5194" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">2p15</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/Q92968" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal membrane protein PEX13</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX13" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX13 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX13" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX13 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX13" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX13</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX13[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX13</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5195" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX14</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5195" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">1p36<wbr style="display:inline-block"></wbr>​.22</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/O75381" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal membrane protein PEX14</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX14" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX14 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX14" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX14 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX14" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX14</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX14[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX14</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/9409" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX16</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=9409" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">11p11<wbr style="display:inline-block"></wbr>​.2</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/Q9Y5Y5" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal membrane protein PEX16</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX16" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX16 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX16" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX16 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX16" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX16</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX16[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX16</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/5824" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX19</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=5824" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">1q23<wbr style="display:inline-block"></wbr>​.2</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/P40855" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisomal biogenesis factor 19</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX19" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX19 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX19" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX19 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX19" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX19</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX19[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX19</a>
|
|
</td></tr><tr><td headers="hd_b_pbd.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="/gene/55670" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
|
<i>PEX26</i>
|
|
</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=55670" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">22q11<wbr style="display:inline-block"></wbr>​.21</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.uniprot.org/uniprot/Q7Z412" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Peroxisome assembly protein 26</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.dbpex.org/index.php?select_db=PEX26" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">dbPEX, PEX26 Gene Database</a>
|
|
<br />
|
|
<a href="http://databases.lovd.nl/shared/genes/PEX26" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX26 database</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PEX26" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX26</a>
|
|
</td><td headers="hd_b_pbd.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=PEX26[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PEX26</a>
|
|
</td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div id="pbd.TFA.1"><p class="no_margin">Data are compiled from the following standard references: gene from
|
|
<a href="http://www.genenames.org/index.html" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">HGNC</a>;
|
|
chromosome locus from
|
|
<a href="http://www.omim.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">OMIM</a>;
|
|
protein from <a href="http://www.uniprot.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">UniProt</a>.
|
|
For a description of databases (Locus Specific, HGMD, ClinVar) to which links are provided, click
|
|
<a href="/books/n/gene/app1/?report=reader">here</a>.</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdmolgenTB"><div id="pbd.molgen.TB" class="table"><h3><span class="label">Table B.</span></h3><div class="caption"><p>OMIM Entries for Zellweger Spectrum Disorder (<a href="/omim/170993,202370,214100,266510,600279,600414,601498,601758,601789,601791,602136,602859,603164,603360,603867,608666" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">View All in OMIM</a>) </p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.molgen.TB/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.molgen.TB_lrgtbl__"><table><tbody><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/170993" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">170993</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 2; PEX2</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/202370" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">202370</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS DISORDER 2B; PBD2B</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/214100" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">214100</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER); PBD1A</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/266510" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">266510</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS DISORDER 3B; PBD3B</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/600279" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">600279</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 19; PEX19</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/600414" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">600414</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 5; PEX5</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/601498" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">601498</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 6; PEX6</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/601758" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">601758</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 12; PEX12</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/601789" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">601789</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 13; PEX13</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/601791" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">601791</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 14; PEX14</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/602136" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">602136</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 1; PEX1</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/602859" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">602859</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 10; PEX10</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/603164" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">603164</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 3; PEX3</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/603360" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">603360</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 16; PEX16</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/603867" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">603867</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 11B; PEX11B</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/608666" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">608666</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">PEROXISOME BIOGENESIS FACTOR 26; PEX26</td></tr></tbody></table></div></div></article><article data-type="table-wrap" id="figobpbdTzellwegerspectrumdisordergenesp"><div id="pbd.T.zellweger_spectrum_disorder_genesp" class="table"><h3><span class="label">Table 8. </span></h3><div class="caption"><p>Zellweger Spectrum Disorder: Gene-Specific Laboratory Considerations</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_genesp/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.zellweger_spectrum_disorder_genesp_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.zellweger_spectrum_disorder_genesp_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Gene <sup>1</sup></th><th id="hd_h_pbd.T.zellweger_spectrum_disorder_genesp_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Special Consideration</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_genesp_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX5</i>
|
|
</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_genesp_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Alternative splicing of the <i>PEX5</i> mRNA produces 2 functional protein variants. The longer variant, PEX5L, contains an additional 37 amino acids compared to the shorter PEX5S [<a class="bibr" href="#pbd.REF.ebberink.2009.93" rid="pbd.REF.ebberink.2009.93">Ebberink et al 2009</a> and references therein]. The reference sequence for PEX5L (<a href="https://www.ncbi.nlm.nih.gov/nuccore/X84899" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">X84899</a> or <a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_001131025.1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_001131025<wbr style="display:inline-block"></wbr>​.1</a>) <sup>2</sup> should be used for sequence analysis.</td></tr><tr><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_genesp_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX6</i>
|
|
</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_genesp_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Common variant in the 3-UTR (<a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">c.*442_445delTAAA</a>) <sup>3</sup></td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.8.1"><p class="no_margin">Genes from <a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object" rid-ob="figobpbdTscreeningassaysforzellwegerspe">Table 1</a> in alphabetic order</p></div></dd></dl><dl class="bkr_refwrap"><dt>2. </dt><dd><div id="pbd.TF.8.2"><p class="no_margin">Sequences of coding region are identical.</p></div></dd></dl><dl class="bkr_refwrap"><dt>3. </dt><dd><div id="pbd.TF.8.3"><p class="no_margin">See <a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object" rid-ob="figobpbdTzellwegerspectrumdisordernotabl">Table 9</a>.</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobpbdTzellwegerspectrumdisordernotabl"><div id="pbd.T.zellweger_spectrum_disorder_notabl" class="table"><h3><span class="label">Table 9. </span></h3><div class="caption"><p>Zellweger Spectrum Disorder: Notable Pathogenic Variants by Gene</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK1448/table/pbd.T.zellweger_spectrum_disorder_notabl/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__pbd.T.zellweger_spectrum_disorder_notabl_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Gene <sup>1</sup></th><th id="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Reference Sequences</th><th id="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">DNA Nucleotide<br />Change (Alias <sup>2</sup>)</th><th id="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_4" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Predicted<br />Protein Change</th><th id="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_5" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Comment [Reference]</th></tr></thead><tbody><tr><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_1" rowspan="2" scope="row" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX1</i>
|
|
</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_2" rowspan="2" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_000466.2" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_000466<wbr style="display:inline-block"></wbr>​.2</a>
|
|
<br />
|
|
<a href="https://www.ncbi.nlm.nih.gov/protein/NP_000457.1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_000457<wbr style="display:inline-block"></wbr>​.1</a>
|
|
</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">c.2097dupT</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Ile700TyrfsTer42</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_5" rowspan="2" colspan="1" style="text-align:left;vertical-align:middle;">Most common <i>PEX1</i> variants; ~80% of persons w/a <i>PEX1</i> pathogenic variant have at least 1 of these common alleles. (See <a href="#pbd.Prevalence">Prevalence</a> & <a href="#pbd.GenotypePhenotype_Correlations">Genotype-Phenotype Correlations</a>.) <sup>3</sup></td></tr><tr><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_3" colspan="1" scope="row" rowspan="1" style="text-align:left;vertical-align:middle;">c.2528G>A</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Gly843Asp</td></tr><tr><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<i>PEX6</i>
|
|
</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_000287.3" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_000287<wbr style="display:inline-block"></wbr>​.3</a>
|
|
<br />
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<a href="https://www.ncbi.nlm.nih.gov/protein/194018488" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_000278<wbr style="display:inline-block"></wbr>​.3</a>
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</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">c.2578C>T</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Arg860Trp</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Assoc w/ZSD in the heterozygous state, acting in an apparent dominant fashion due to allelic expression imbalance assoc w/common variant <a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_000287.3" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_000287<wbr style="display:inline-block"></wbr>​.3</a>:c.*442_445delTAAA in the 3' UTR that disrupts 1 of 2 polyadenylation sites. Persons who have c.*442_445delTAAA on both chromosomes are unaffected; but those who have c.2578C>T (p.Arg860Trp) on the c.*442_445delTAAA background but lack c.*442_445delTAAA on the opposite chromosome have a 2- to 3-fold ↑ in abnormal PEX6 (compared to controls) & biochemical & clinical features consistent w/ZSD [<a class="bibr" href="#pbd.REF.falkenberg.2017.965" rid="pbd.REF.falkenberg.2017.965">Falkenberg et al 2017</a>].</td></tr><tr><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>PEX10</i>
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</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<a href="https://www.ncbi.nlm.nih.gov/nuccore/24797087" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_002617<wbr style="display:inline-block"></wbr>​.3</a>
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<br />
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<a href="https://www.ncbi.nlm.nih.gov/protein/4505715" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_002608<wbr style="display:inline-block"></wbr>​.1</a>
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</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">c.814_815delCT<br />(PEX10Δ814/815)</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_4" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">p.Leu272ValfsTer66</td><td headers="hd_h_pbd.T.zellweger_spectrum_disorder_notabl_1_1_1_5" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Common allele in the Japanese population, where it appears to have arisen once on an ancestral haplotype [<a class="bibr" href="#pbd.REF.shimozawa.2003.40" rid="pbd.REF.shimozawa.2003.40">Shimozawa et al 2003</a>]</td></tr></tbody></table></div><div class="tblwrap-foot"><div><dl class="temp-labeled-list small"><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin">Variants listed in the table have been provided by the authors. <i>GeneReviews</i> staff have not independently verified the classification of variants.</p></div></dd></dl><dl class="bkr_refwrap"><dt></dt><dd><div><p class="no_margin"><i>GeneReviews</i> follows the standard naming conventions of the Human Genome Variation Society (<a href="https://varnomen.hgvs.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">varnomen<wbr style="display:inline-block"></wbr>​.hgvs.org</a>). See <a href="/books/n/gene/app3/?report=reader">Quick Reference</a> for an explanation of nomenclature.</p></div></dd></dl><dl class="bkr_refwrap"><dt>1. </dt><dd><div id="pbd.TF.9.1"><p class="no_margin">Genes from <a href="/books/NBK1448/table/pbd.T.screening_assays_for_zellweger_spe/?report=objectonly" target="object" rid-ob="figobpbdTscreeningassaysforzellwegerspe">Table 1</a> in alphabetic order</p></div></dd></dl><dl class="bkr_refwrap"><dt>2. </dt><dd><div id="pbd.TF.9.2"><p class="no_margin">Variant designation that does not conform to current naming conventions</p></div></dd></dl><dl class="bkr_refwrap"><dt>3. </dt><dd><div id="pbd.TF.9.3"><p class="no_margin">It has been proposed that the two common alleles reside on specific haplotypes and arose as founder variants [<a class="bibr" href="#pbd.REF.collins.1999.45" rid="pbd.REF.collins.1999.45">Collins & Gould 1999</a>], suggesting that these sites are not hot spots for recurrent pathogenic variants.</p></div></dd></dl></dl></div></div></div></article></div><div id="jr-scripts"><script src="/corehtml/pmc/jatsreader/ptpmc_3.22/js/libs.min.js"> </script><script src="/corehtml/pmc/jatsreader/ptpmc_3.22/js/jr.min.js"> </script><script type="text/javascript">if (typeof (jQuery) != 'undefined') { (function ($) { $(function () { var min = Math.ceil(1); var max = Math.floor(100000); var randomNum = Math.floor(Math.random() * (max - min)) + min; var surveyUrl = "/projects/Gene/portal/surveys/seqdbui-survey.js?rando=" + randomNum.toString(); $.getScript(surveyUrl, function () { try { ncbi.seqDbUISurvey.init(); } catch (err) { console.info(err); } }).fail(function (jqxhr, settings, exception) { console.info('Cannot load survey script', jqxhr); });; }); })(jQuery); };</script></div></div>
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