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<script type="text/javascript" src="/corehtml/pmc/jatsreader/ptpmc_3.22/js/jr.boots.min.js"> </script><title>SYNGAP1-Related Intellectual Disability - 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="SYNGAP1-Related Intellectual Disability">
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<meta name="citation_publisher" content="University of Washington, Seattle">
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<meta name="citation_date" content="2019/02/21">
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<meta name="citation_author" content="J Lloyd Holder, Jr">
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<meta name="citation_author" content="Fadi F Hamdan">
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<meta name="citation_author" content="Jacques L Michaud">
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<meta name="citation_keywords" content="SYNGAP1-Related Developmental and Epileptic Encephalopathy">
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<meta name="citation_keywords" content="SYNGAP1-Related Developmental and Epileptic Encephalopathy">
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<meta name="citation_keywords" content="Ras/Rap GTPase-activating protein SynGAP">
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<meta name="citation_keywords" content="SYNGAP1">
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<meta name="citation_keywords" content="SYNGAP1-Related Intellectual Disability">
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<meta name="DC.Title" content="SYNGAP1-Related Intellectual Disability">
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<meta name="DC.Publisher" content="University of Washington, Seattle">
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<meta name="DC.Contributor" content="J Lloyd Holder, Jr">
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<meta name="DC.Contributor" content="Fadi F Hamdan">
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<meta name="DC.Contributor" content="Jacques L Michaud">
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<meta name="DC.Date" content="2019/02/21">
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<meta name="description" content="SYNGAP1-related intellectual disability (SYNGAP1-ID) is characterized by developmental delay (DD) or intellectual disability (ID) (100% of affected individuals), generalized epilepsy (~84%), and autism spectrum disorder (ASD) and other behavioral abnormalities (≤50%). To date more than 50 individuals with SYNGAP1-ID have been reported. In the majority DD/ID was moderate to severe; in some it was mild. The epilepsy is generalized; a subset of individuals with epilepsy have myoclonic astatic epilepsy (Doose syndrome) or epilepsy with myoclonic absences. Behavioral abnormalities can include stereotypic behaviors (e.g., hand flapping, obsessions with certain objects) as well as poor social development. Feeding difficulties can be significant in some.">
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<meta name="og:description" content="SYNGAP1-related intellectual disability (SYNGAP1-ID) is characterized by developmental delay (DD) or intellectual disability (ID) (100% of affected individuals), generalized epilepsy (~84%), and autism spectrum disorder (ASD) and other behavioral abnormalities (≤50%). To date more than 50 individuals with SYNGAP1-ID have been reported. In the majority DD/ID was moderate to severe; in some it was mild. The epilepsy is generalized; a subset of individuals with epilepsy have myoclonic astatic epilepsy (Doose syndrome) or epilepsy with myoclonic absences. Behavioral abnormalities can include stereotypic behaviors (e.g., hand flapping, obsessions with certain objects) as well as poor social development. Feeding difficulties can be significant in some.">
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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="_NBK537721_"><span class="title" itemprop="name"><i>SYNGAP1</i>-Related Intellectual Disability</span></h1><div itemprop="alternativeHeadline" class="subtitle whole_rhythm">Synonym: <i>SYNGAP1</i>-Related Developmental and Epileptic Encephalopathy</div><p class="contribs">Holder JL Jr, Hamdan FF, Michaud JL.</p><p class="fm-aai"><a href="#_NBK537721_pubdet_">Publication Details</a></p><p><em>Estimated reading time: 17 minutes</em></p></div></div><div class="jig-ncbiinpagenav body-content whole_rhythm" data-jigconfig="allHeadingLevels: ['h2'],smoothScroll: false" itemprop="text"><div id="syngap1-id.Summary" itemprop="description"><h2 id="_syngap1-id_Summary_">Summary</h2><div><h4 class="inline">Clinical characteristics.</h4><p><i>SYNGAP1</i>-related intellectual disability (<i>SYNGAP1-</i>ID) is characterized by developmental delay (DD) or intellectual disability (ID) (100% of affected individuals), generalized epilepsy (~84%), and autism spectrum disorder (ASD) and other behavioral abnormalities (≤50%). To date more than 50 individuals with <i>SYNGAP1-</i>ID have been reported. In the majority DD/ID was moderate to severe; in some it was mild. The epilepsy is generalized; a subset of individuals with epilepsy have myoclonic astatic epilepsy (Doose syndrome) or epilepsy with myoclonic absences. Behavioral abnormalities can include stereotypic behaviors (e.g., hand flapping, obsessions with certain objects) as well as poor social development. Feeding difficulties can be significant in some.</p></div><div><h4 class="inline">Diagnosis/testing.</h4><p>The diagnosis of <i>SYNGAP1-</i>ID is established in a proband with developmental delay or intellectual disability in whom molecular genetic testing identifies either a heterozygous pathogenic variant in <i>SYNGAP1</i> (~89%) or a deletion of 6p21.3 (~11%).</p></div><div><h4 class="inline">Management.</h4><p><i>Treatment of manifestations:</i> DD/ID are managed as per standard practice. No guidelines are available regarding choice of specific anti-seizure medications (ASMs). In about 50% of patients, the epilepsy responds to a single ASM; in the remainder it is pharmacoresistant. Children may qualify for and benefit from interventions used in treatment of ASD. Consultation with a developmental pediatrician may guide parents through appropriate behavioral management strategies and/or provide prescription medications when necessary. Nasogastric/gastrostomy feeding may be required for individuals with persistent feeding issues.</p><p><i>Surveillance:</i> Monitor seizure manifestations and control; behavioral issues; developmental progress and educational needs.</p></div><div><h4 class="inline">Genetic counseling.</h4><p><i>SYNGAP1-</i>ID is inherited in an autosomal dominant manner. To date almost all probands with <i>SYNGAP1-</i>ID whose parents have undergone molecular genetic testing have had a <i>de novo</i> germline pathogenic variant; however, vertical transmission (from a mildly affected, mosaic parent to the proband) has been reported in one family. Thus, while the risk to sibs appears to be low, it is presumed to be greater than in the general population because of the possibility of germline mosaicism in a parent. Once the <i>SYNGAP1</i> pathogenic variant has been identified in an affected family member, prenatal testing for a pregnancy at increased risk and preimplantation genetic testing are possible.</p></div></div><div id="syngap1-id.Diagnosis"><h2 id="_syngap1-id_Diagnosis_">Diagnosis</h2><p>No formal diagnostic criteria have been published for <i>SYNGAP1</i>-related intellectual disability.</p><div id="syngap1-id.Suggestive_Findings"><h3>Suggestive Findings</h3><p><i>SYNGAP1</i>-related intellectual disability (<i>SYNGAP1-</i>ID) <b>should be considered</b> in individuals with developmental delay or intellectual disability with or without:</p><ul><li class="half_rhythm"><div>Generalized epilepsy;</div><div>and/or</div></li><li class="half_rhythm"><div>Autism spectrum disorder (ASD).</div></li></ul></div><div id="syngap1-id.Establishing_the_Diagnosis"><h3>Establishing the Diagnosis</h3><p>The diagnosis of <i>SYNGAP1-</i>ID <b>is established</b> in a proband with developmental delay (DD) or intellectual disability (ID) in whom molecular genetic testing (see <a href="/books/NBK537721/table/syngap1-id.T.molecular_genetic_testing_u/?report=objectonly" target="object" rid-ob="figobsyngap1idTmoleculargenetictestingu">Table 1</a>) identifies either:</p><ul><li class="half_rhythm"><div>A heterozygous pathogenic (or likely pathogenic) variant in <i>SYNGAP1</i> (~89%);</div><div>or</div></li><li class="half_rhythm"><div>A deletion of 6p21.3 (~11%).</div></li></ul><p>Note: 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="#syngap1-id.REF.richards.2015.405" rid="syngap1-id.REF.richards.2015.405">Richards et al 2015</a>]. Reference to "pathogenic variants" in this section is understood to include any likely pathogenic variants.</p><p><b>Molecular genetic testing</b> in a child with DD or an older individual with ID typically begins with chromosomal microarray analysis (CMA). If CMA is not diagnostic, the next step is typically either a multigene panel or exome sequencing. Note: Single-gene testing (sequence analysis of <i>SYNGAP1</i>, followed by gene-targeted deletion/duplication analysis) is rarely useful and typically NOT recommended.</p><p><b>CMA</b> uses oligonucleotide or SNP arrays to detect genome-wide large deletions/duplications (including <i>SYNGAP1</i>) that cannot be detected by sequence analysis. Note: The ability to determine the size of the deletion/duplication depends on the type of microarray used and the density of probes in the 6p21.32 region.</p><p><b>An ID multigene panel</b> that includes <i>SYNGAP1</i> and other genes of interest (see <a href="#syngap1-id.Differential_Diagnosis">Differential Diagnosis</a>) is most likely to identify the genetic cause of the condition in a person with a nondiagnostic CMA 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. For this disorder, an ID multigene panel that also includes deletion/duplication analysis is recommended (see <a href="/books/NBK537721/table/syngap1-id.T.molecular_genetic_testing_u/?report=objectonly" target="object" rid-ob="figobsyngap1idTmoleculargenetictestingu">Table 1</a>).</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><p><b>Exome sequencing,</b> which does not require the clinician to determine which gene is likely involved, has the advantage over an ID multigene panel of detecting variants in recently identified rare genes not yet included in some ID multigene panels.</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="figsyngap1idTmoleculargenetictestingu"><a href="/books/NBK537721/table/syngap1-id.T.molecular_genetic_testing_u/?report=objectonly" target="object" title="Table 1. " class="img_link icnblk_img" rid-ob="figobsyngap1idTmoleculargenetictestingu"><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="syngap1-id.T.molecular_genetic_testing_u"><a href="/books/NBK537721/table/syngap1-id.T.molecular_genetic_testing_u/?report=objectonly" target="object" rid-ob="figobsyngap1idTmoleculargenetictestingu">Table 1. </a></h4><p class="float-caption no_bottom_margin">Molecular Genetic Testing Used in <i>SYNGAP1</i>-Related Intellectual Disability </p></div></div></div></div><div id="syngap1-id.Clinical_Characteristics"><h2 id="_syngap1-id_Clinical_Characteristics_">Clinical Characteristics</h2><div id="syngap1-id.Clinical_Description"><h3>Clinical Description</h3><p>Since the original description of <i>SYNGAP1</i>-related intellectual disability (<i>SYNGAP1-</i>ID) in three individuals [<a class="bibr" href="#syngap1-id.REF.hamdan.2009.599" rid="syngap1-id.REF.hamdan.2009.599">Hamdan et al 2009</a>], more than 50 affected individuals with detailed clinical information have been reported [<a class="bibr" href="#syngap1-id.REF.krepischi.2010.2376" rid="syngap1-id.REF.krepischi.2010.2376">Krepischi et al 2010</a>, <a class="bibr" href="#syngap1-id.REF.pinto.2010.368" rid="syngap1-id.REF.pinto.2010.368">Pinto et al 2010</a>, <a class="bibr" href="#syngap1-id.REF.vissers.2010.1109" rid="syngap1-id.REF.vissers.2010.1109">Vissers et al 2010</a>, <a class="bibr" href="#syngap1-id.REF.hamdan.2011a.898" rid="syngap1-id.REF.hamdan.2011a.898">Hamdan et al 2011a</a>, <a class="bibr" href="#syngap1-id.REF.hamdan.2011b.306" rid="syngap1-id.REF.hamdan.2011b.306">Hamdan et al 2011b</a>, <a class="bibr" href="#syngap1-id.REF.klitten.2011.e190" rid="syngap1-id.REF.klitten.2011.e190">Klitten et al 2011</a>, <a class="bibr" href="#syngap1-id.REF.zollino.2011.239" rid="syngap1-id.REF.zollino.2011.239">Zollino et al 2011</a>, <a class="bibr" href="#syngap1-id.REF.de_ligt.2012.1921" rid="syngap1-id.REF.de_ligt.2012.1921">de Ligt et al 2012</a>, <a class="bibr" href="#syngap1-id.REF.rauch.2012.1674" rid="syngap1-id.REF.rauch.2012.1674">Rauch et al 2012</a>, <a class="bibr" href="#syngap1-id.REF.berryer.2013.385" rid="syngap1-id.REF.berryer.2013.385">Berryer et al 2013</a>, <a class="bibr" href="#syngap1-id.REF.carvill.2013.825" rid="syngap1-id.REF.carvill.2013.825">Carvill et al 2013</a>, <a class="bibr" href="#syngap1-id.REF.writzl.2013.1682" rid="syngap1-id.REF.writzl.2013.1682">Writzl & Knegt 2013</a>, <a class="bibr" href="#syngap1-id.REF.redin.2014.724" rid="syngap1-id.REF.redin.2014.724">Redin et al 2014</a>, <a class="bibr" href="#syngap1-id.REF.parker.2015.2231" rid="syngap1-id.REF.parker.2015.2231">Parker et al 2015</a>, <a class="bibr" href="#syngap1-id.REF.mignot.2016.511" rid="syngap1-id.REF.mignot.2016.511">Mignot et al 2016</a>, <a class="bibr" href="#syngap1-id.REF.prchalova.2017.62" rid="syngap1-id.REF.prchalova.2017.62">Prchalova et al 2017</a>]. The following description of the phenotypic features associated with this condition is based on these reports.</p><p><b>Developmental delay and intellectual disability.</b> The great majority of affected children present with developmental delay or intellectual disability that is typically moderate to severe but can be mild.</p><p>Early motor development is characterized by hypotonia. The average age at walking was 26 months (range: 10.5 months to 5 years). A subset of these children had an ataxic gait that remained stable or improved over time.</p><p>Language is generally impaired; a third of individuals age five years or more remain nonverbal. In those who are verbal, language development ranges from use of single words only to four-to-five-word sentences.</p><p><b>Epilepsy.</b> Approximately 84% of individuals with <i>SYNGAP1-</i>ID have generalized epilepsy; a subset of these were diagnosed with myoclonic astatic epilepsy (Doose syndrome) or epilepsy with myoclonic absences [<a class="bibr" href="#syngap1-id.REF.mignot.2016.511" rid="syngap1-id.REF.mignot.2016.511">Mignot et al 2016</a>].</p><p>While the epilepsy responds to a single anti-seizure medication in approximately half of affected individuals, it is pharmacoresistant in the remainder. Children with refractory seizures may be diagnosed with epileptic encephalopathy (i.e., refractory seizures and cognitive slowing or regression associated with frequent ongoing epileptiform activity).</p><ul><li class="half_rhythm"><div><b>Age at onset of seizures</b> varies between six months and seven years; mean age of seizure onset was 3.5 years in one study [<a class="bibr" href="#syngap1-id.REF.mignot.2016.511" rid="syngap1-id.REF.mignot.2016.511">Mignot et al 2016</a>].</div></li><li class="half_rhythm"><div><b>Seizure types</b> include typical or atypical seizures, myoclonic jerks with or without falls, eyelid myoclonia, tonic-clonic seizures, myoclonic absences, and atonic seizures. In one study, Doose syndrome (myoclonic astatic epilepsy) was diagnosed in three of 17 individuals [<a class="bibr" href="#syngap1-id.REF.mignot.2016.511" rid="syngap1-id.REF.mignot.2016.511">Mignot et al 2016</a>].</div></li><li class="half_rhythm"><div><b>Electroencephalography</b> typically shows generalized epileptic activity, frequently with a posterior predominance. Photosensitivity and fixation-off phenomenon have been observed in a number of individuals.</div></li><li class="half_rhythm"><div><b>Brain MRI</b> is typically normal; in rare cases, brain atrophy or delayed myelination has been reported.</div></li></ul><p><b>Autism spectrum disorder (ASD) and other behavioral abnormalities.</b> The occurrence of ASD could be as high as 50%. This includes stereotypic behaviors such as hand flapping, obsessions with certain objects, and poor social development. In addition, inattention, impulsivity, self-directed and other-directed aggressive behavior, elevated pain threshold, hyperacusis, and sleep disorders have been observed.</p><p><b>Other associated features</b> include the following:</p><ul><li class="half_rhythm"><div><b>Acquired microcephaly</b> observed in a minority of affected individuals</div></li><li class="half_rhythm"><div><b>Eye abnormalities</b> including strabismus</div></li><li class="half_rhythm"><div><b>Musculoskeletal disorders</b> including hip rotation or dysplasia, kyphoscoliosis, and <i>pes planus</i></div></li><li class="half_rhythm"><div><b>Hypertrichosis</b> (predominantly on the limbs and lower spine) occasionally described</div></li><li class="half_rhythm"><div><b>Gastrointestinal dysfunction</b> (including constipation requiring medical intervention) frequently reported; swallowing difficulties rarely reported</div></li><li class="half_rhythm"><div><b>Craniofacial features.</b> Although some authors have suggested a subtle but consistent facial appearance (almond-shaped palpebral fissures, mildly myopathic and open-mouthed appearance) [<a class="bibr" href="#syngap1-id.REF.parker.2015.2231" rid="syngap1-id.REF.parker.2015.2231">Parker et al 2015</a>], it is unclear if these changes are distinct enough to allow a clinician to suspect the condition in a child.</div></li></ul><p><b>Life span.</b> It is unknown if life span in <i>SYNGAP1-</i>ID is abnormal. One reported individual is alive at age 31 years [<a class="bibr" href="#syngap1-id.REF.prchalova.2017.62" rid="syngap1-id.REF.prchalova.2017.62">Prchalova et al 2017</a>], demonstrating that survival into adulthood is possible. Since many adults with disabilities have not undergone advanced genetic testing, it is likely that adults with this condition are underrecognized and underreported.</p></div><div id="syngap1-id.GenotypePhenotype_Correlation"><h3>Genotype-Phenotype Correlations</h3><p>No definitive phenotype-genotype correlation between the type of <i>SYNGAP1</i> pathogenic variant (missense, truncating, large intragenic deletion) and cognitive abilities or the occurrence of comorbidities has been observed.</p></div><div id="syngap1-id.Penetrance"><h3>Penetrance</h3><p>Penetrance is 100%. All individuals with germline pathogenic variants in <i>SYNGAP1</i> have developmental delay, cognitive dysfunction, intellectual disability, and/or epilepsy.</p></div><div id="syngap1-id.Prevalence"><h3>Prevalence</h3><p>The prevalence of <i>SYNGAP1</i> pathogenic variants in two studies was:</p><ul><li class="half_rhythm"><div>1% in a series of 500 individuals with epileptic encephalopathy [<a class="bibr" href="#syngap1-id.REF.carvill.2013.825" rid="syngap1-id.REF.carvill.2013.825">Carvill et al 2013</a>];</div></li><li class="half_rhythm"><div>0.75% in a large series of 931 unrelated children with intellectual disability [<a class="bibr" href="#syngap1-id.REF.fitzgerald.2015.223" rid="syngap1-id.REF.fitzgerald.2015.223">Fitzgerald et al 2015</a>].</div></li></ul></div></div><div id="syngap1-id.Genetically_Related_Allelic_D"><h2 id="_syngap1-id_Genetically_Related_Allelic_D_">Genetically Related (Allelic) Disorders</h2><p>No phenotypes other than those discussed in this <i>GeneReview</i> are known to be associated with germline pathogenic variants in <i>SYNGAP1</i>.</p></div><div id="syngap1-id.Differential_Diagnosis"><h2 id="_syngap1-id_Differential_Diagnosis_">Differential Diagnosis</h2><p>The phenotype associated with <i>SYNGAP1</i>-related intellectual disability (ID) overlaps with that of other disorders of ID and epileptic encephalopathy.</p><p>Most genes known to be associated with ID (see <a href="https://omim.org/phenotypicSeries/PS156200" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">OMIM Autosomal Dominant Intellectual Developmental Disorder Phenotypic Series</a>) and epileptic encephalopathy (see <a href="http://omim.org/phenotypicSeries/PS308350" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">OMIM Epileptic Encephalopathy, Early Infantile Phenotypic Series</a>) if compatible with walking should be included in the differential diagnosis.</p></div><div id="syngap1-id.Management"><h2 id="_syngap1-id_Management_">Management</h2><div id="syngap1-id.Evaluations_Following_Initial"><h3>Evaluations Following Initial Diagnosis</h3><p>To establish the extent of disease and needs in an individual diagnosed with <i>SYNGAP1</i>-related intellectual disability, the evaluations summarized in <a href="/books/NBK537721/table/syngap1-id.T.recommended_evaluations_fol/?report=objectonly" target="object" rid-ob="figobsyngap1idTrecommendedevaluationsfol">Table 2</a> (if not performed as part of the evaluation that led to diagnosis) are recommended.</p><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figsyngap1idTrecommendedevaluationsfol"><a href="/books/NBK537721/table/syngap1-id.T.recommended_evaluations_fol/?report=objectonly" target="object" title="Table 2. " class="img_link icnblk_img" rid-ob="figobsyngap1idTrecommendedevaluationsfol"><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="syngap1-id.T.recommended_evaluations_fol"><a href="/books/NBK537721/table/syngap1-id.T.recommended_evaluations_fol/?report=objectonly" target="object" rid-ob="figobsyngap1idTrecommendedevaluationsfol">Table 2. </a></h4><p class="float-caption no_bottom_margin">Recommended Evaluations Following Initial Diagnosis in Individuals with <i>SYNGAP1</i>-Related Intellectual Disability </p></div></div></div><div id="syngap1-id.Treatment_of_Manifestations"><h3>Treatment of Manifestations</h3><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figsyngap1idTtreatmentofmanifestations"><a href="/books/NBK537721/table/syngap1-id.T.treatment_of_manifestations/?report=objectonly" target="object" title="Table 3. " class="img_link icnblk_img" rid-ob="figobsyngap1idTtreatmentofmanifestations"><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="syngap1-id.T.treatment_of_manifestations"><a href="/books/NBK537721/table/syngap1-id.T.treatment_of_manifestations/?report=objectonly" target="object" rid-ob="figobsyngap1idTtreatmentofmanifestations">Table 3. </a></h4><p class="float-caption no_bottom_margin">Treatment of Manifestations in Individuals with <i>SYNGAP1</i>-Related Intellectual Disability </p></div></div><p>Education of parents regarding common seizure presentations is appropriate. For information on non-medical interventions and coping strategies for parents or caregivers of children diagnosed with epilepsy, see <a href="https://www.epilepsy.com/tools-resources/forms-resources#Epilepsy-Foundation-Toolbox" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Epilepsy Foundation Toolbox</a>.</p><div id="syngap1-id.Developmental_Delay__Intellec"><h4>Developmental Delay / Intellectual Disability Management Issues</h4><p>The following information represents typical management recommendations for individuals with developmental delay / intellectual disability in the United States; standard recommendations may vary from country to country.</p><p><b>Ages 0-3 years.</b> Referral to an early intervention program is recommended for access to occupational, physical, speech, and feeding therapy. In the US, early intervention is a federally funded program available in all states.</p><p><b>Ages 3-5 years.</b> In the US, developmental preschool through the local public school district is recommended. Before placement, an evaluation is made to determine needed services and therapies and an individualized education plan (IEP) is developed.</p><p>
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<b>Ages 5-21 years</b>
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</p><ul><li class="half_rhythm"><div>In the US, an IEP based on the individual's level of function should be developed by the local public school district. Affected children are permitted to remain in the public school district until age 21.</div></li><li class="half_rhythm"><div>Discussion about transition plans including financial, vocation/employment, and medical arrangements should begin at age 12 years. Developmental pediatricians can provide assistance with transition to adulthood.</div></li></ul><p><b>All ages.</b> Consultation with a developmental pediatrician is recommended to ensure the involvement of appropriate community, state, and educational agencies and to support parents in maximizing quality of life.</p><p>Consideration of private supportive therapies based on the affected individual's needs is recommended. Specific recommendations regarding type of therapy can be made by a developmental pediatrician.</p><p>In the US:</p><ul><li class="half_rhythm"><div>Developmental Disabilities Administration (DDA) enrollment is recommended. DDA is a public agency that provides services and support to qualified individuals. Eligibility differs by state but is typically determined by diagnosis and/or associated cognitive/adaptive disabilities.</div></li><li class="half_rhythm"><div>Families with limited income and resources may also qualify for supplemental security income (SSI) for their child with a disability.</div></li></ul></div><div id="syngap1-id.Motor_Dysfunction"><h4>Motor Dysfunction</h4><p>
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<b>Gross motor dysfunction</b>
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</p><ul><li class="half_rhythm"><div>Physical therapy is recommended to maximize mobility and to reduce the risk for later-onset orthopedic complications (e.g., contractures, scoliosis, hip dislocation).</div></li><li class="half_rhythm"><div>Consider use of durable medical equipment as needed (e.g., wheelchairs, walkers, bath chairs, orthotics, adaptive strollers).</div></li></ul><p><b>Fine motor dysfunction.</b> Occupational therapy is recommended for difficulty with fine motor skills that affect adaptive function such as feeding, grooming, dressing, and writing.</p><p><b>Oral motor dysfunction.</b> Assuming that the individual is safe to eat by mouth, feeding therapy – typically from an occupational or speech therapist – is recommended for affected individuals who have difficulty feeding because of poor oral motor control.</p><p><b>Communication issues.</b> Consider evaluation for alternative means of communication (e.g., <a href="https://www.asha.org/NJC/AAC/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">augmentative and alternative communication</a> [AAC]) for individuals who have expressive language difficulties.</p></div><div id="syngap1-id.SocialBehavioral_Concerns"><h4>Social/Behavioral Concerns</h4><p>Children may qualify for and benefit from interventions used in treatment of autism spectrum disorder, including applied behavior analysis (ABA). ABA therapy is targeted to the individual child's behavioral, social, and adaptive strengths and weaknesses and is typically performed one on one with a board-certified behavior analyst.</p><p>Consultation with a developmental pediatrician may be helpful in guiding parents through appropriate behavior management strategies or providing prescription medications when necessary.</p><p>Concerns about serious aggressive or destructive behavior can be addressed by a pediatric psychiatrist.</p></div></div><div id="syngap1-id.Surveillance"><h3>Surveillance</h3><p>Monitor those with seizures as clinically indicated.</p><p>Assess as needed for anxiety, attention, and aggressive or self-injurious behavior.</p><p>Monitor developmental progress and educational needs.</p></div><div id="syngap1-id.Evaluation_of_Relatives_at_Ri"><h3>Evaluation of Relatives at Risk</h3><p>See <a href="#syngap1-id.Related_Genetic_Counseling_Is">Genetic Counseling</a> for issues related to testing of at-risk relatives for genetic counseling purposes.</p></div><div id="syngap1-id.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="syngap1-id.Genetic_Counseling"><h2 id="_syngap1-id_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="syngap1-id.Mode_of_Inheritance"><h3>Mode of Inheritance</h3><p><i>SYNGAP1</i>-related intellectual disability (<i>SYNGAP1-</i>ID) is inherited in an autosomal dominant manner and is typically caused by a <i>de novo</i> pathogenic variant.</p></div><div id="syngap1-id.Risk_to_Family_Members"><h3>Risk to Family Members</h3><p>
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<b>Parents of a proband</b>
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</p><ul><li class="half_rhythm"><div>Almost all probands with <i>SYNGAP1-</i>ID reported to date whose parents have undergone molecular genetic testing have the disorder as a result of a <i>de novo</i> germline pathogenic variant.</div></li><li class="half_rhythm"><div>Vertical transmission (from a mildly affected, mosaic parent to the proband) has been reported in one family to date [<a class="bibr" href="#syngap1-id.REF.berryer.2013.385" rid="syngap1-id.REF.berryer.2013.385">Berryer et al 2013</a>].</div></li><li class="half_rhythm"><div>Molecular genetic testing is recommended for the parents of a proband with an apparent <i>de novo</i> pathogenic variant.</div></li><li class="half_rhythm"><div>If the pathogenic variant found in the proband cannot be detected in the leukocyte DNA of either parent, the proband most likely has a <i>de novo</i> pathogenic variant. Parental germline mosaicism is also a possible explanation; paternal somatic and germline mosaicism has been reported in one family [<a class="bibr" href="#syngap1-id.REF.berryer.2013.385" rid="syngap1-id.REF.berryer.2013.385">Berryer et al 2013</a>].</div></li><li class="half_rhythm"><div>Note: If the parent is the individual in whom the pathogenic variant first occurred, the parent may have both somatic and germline mosaicism for the variant and may be mildly affected [<a class="bibr" href="#syngap1-id.REF.berryer.2013.385" rid="syngap1-id.REF.berryer.2013.385">Berryer et al 2013</a>].</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>The risk to the sibs of the proband depends on the genetic status of the proband's parents.</div></li><li class="half_rhythm"><div>Most affected individuals reported to date have had a <i>de novo</i>
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<i>SYNGAP1</i> pathogenic variant, suggesting a low risk to sibs. However, because of the possibility of germline mosaicism in a parent, the risk is presumed to be greater than in the general population [<a class="bibr" href="#syngap1-id.REF.berryer.2013.385" rid="syngap1-id.REF.berryer.2013.385">Berryer et al 2013</a>].</div></li></ul><p><b>Offspring of a proband.</b> Individuals with <i>SYNGAP1</i>-ID are not known to reproduce; the theoretic risk to offspring of mildly affected mosaic individuals [<a class="bibr" href="#syngap1-id.REF.berryer.2013.385" rid="syngap1-id.REF.berryer.2013.385">Berryer et al 2013</a>] is up to 50%.</p><p><b>Other family members.</b> Given that most probands with <i>SYNGAP1-</i>ID reported to date have the disorder as a result of a <i>de novo</i> pathogenic variant, the risk to other family members is presumed to be low.</p></div><div id="syngap1-id.Related_Genetic_Counseling_Is"><h3>Related Genetic Counseling Issues</h3><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 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 parents of affected individuals.</div></li></ul></div><div id="syngap1-id.Prenatal_Testing_and_Preimpla"><h3>Prenatal Testing and Preimplantation Genetic Testing</h3><p>Once the <i>SYNGAP1</i> pathogenic variant has been identified in an affected family member, prenatal and preimplantation genetic testing are possible.</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="syngap1-id.Resources"><h2 id="_syngap1-id_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>MedlinePlus</b>
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</div><div>
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<a href="http://www.nlm.nih.gov/medlineplus/ency/article/001523.htm" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Intellectual Disability</a>
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</div></li><li class="half_rhythm"><div>
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<b>SYNGAP1 Foundation</b>
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</div><div><b>Phone:</b> 240-347-0302</div><div><b>Email:</b> admin@syngap1foundation.org</div><div>
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<a href="https://syngap1foundation.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">www.syngap1foundation.org</a>
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</div></li><li class="half_rhythm"><div>
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<b>VOR: Speaking out for people with intellectual and developmental disabilities</b>
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</div><div><b>Phone:</b> 877-399-4867</div><div><b>Email:</b> info@vor.net</div><div>
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<a href="http://www.vor.net/index.php" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">vor.net</a>
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</div></li><li class="half_rhythm"><div>
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<b>American Association on Intellectual and Developmental Disabilities (AAIDD)</b>
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</div><div><b>Phone:</b> 202-387-1968</div><div>
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<a href="https://www.aaidd.org" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">aaidd.org</a>
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</div></li><li class="half_rhythm"><div>
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<b>CDC - Child Development</b>
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</div><div><b>Phone:</b> 800-232-4636</div><div>
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<a href="https://www.cdc.gov/child-development/about/developmental-disability-basics.html" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Developmental Disability Basics</a>
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</div></li><li class="half_rhythm"><div>
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<b>VOR: Speaking out for people with intellectual and developmental disabilities</b>
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</div><div><b>Phone:</b> 877-399-4867</div><div><b>Email:</b> info@vor.net</div><div>
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<a href="http://www.vor.net/index.php" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">vor.net</a>
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</div></li><li class="half_rhythm"><div>
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<b>SYNGAP1 (MRD5) Patient Registry</b>
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</div><div>
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<a href="https://syngap1registry.iamrare.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">www.syngap1registry.iamrare.org</a>
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</div></li></ul>
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</div><div id="syngap1-id.Molecular_Genetics"><h2 id="_syngap1-id_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="figsyngap1idmolgenTA"><a href="/books/NBK537721/table/syngap1-id.molgen.TA/?report=objectonly" target="object" title="Table A." class="img_link icnblk_img" rid-ob="figobsyngap1idmolgenTA"><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="syngap1-id.molgen.TA"><a href="/books/NBK537721/table/syngap1-id.molgen.TA/?report=objectonly" target="object" rid-ob="figobsyngap1idmolgenTA">Table A.</a></h4><p class="float-caption no_bottom_margin">SYNGAP1-Related Intellectual Disability: Genes and Databases </p></div></div><div class="iconblock whole_rhythm clearfix ten_col table-wrap" id="figsyngap1idmolgenTB"><a href="/books/NBK537721/table/syngap1-id.molgen.TB/?report=objectonly" target="object" title="Table B." class="img_link icnblk_img" rid-ob="figobsyngap1idmolgenTB"><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="syngap1-id.molgen.TB"><a href="/books/NBK537721/table/syngap1-id.molgen.TB/?report=objectonly" target="object" rid-ob="figobsyngap1idmolgenTB">Table B.</a></h4><p class="float-caption no_bottom_margin">OMIM Entries for SYNGAP1-Related Intellectual Disability (View All in OMIM) </p></div></div><p><b>Gene structure.</b> To date two NCBI reference sequences for human <i>SYNGAP1</i> have been reported:</p><ul><li class="half_rhythm"><div><a href="https://www.ncbi.nlm.nih.gov/nuccore/194248067" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_006772.2</a> (isoform 1) consists of 19 exons and encodes a protein of 1,343 amino acids (<a href="https://www.ncbi.nlm.nih.gov/protein/NP_006763.2" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_006763.2</a>).</div></li><li class="half_rhythm"><div><a href="https://www.ncbi.nlm.nih.gov/nuccore/194248069" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NM_001130066.1</a> (isoform 2) consists of 18 exons resulting in a protein of 1,292 amino acids (<a href="https://www.ncbi.nlm.nih.gov/protein/NP_001123538.1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NP_001123538.1</a>).</div></li></ul><p>Molecular genetic testing for <i>SYNGAP1</i> pathogenic variants should include all 19 exons present in its largest reference sequence isoform (NM_006772.2).</p><p>By comparing human and rodent <i>SYNGAP1</i> cDNAs, <a class="bibr" href="#syngap1-id.REF.mignot.2016.511" rid="syngap1-id.REF.mignot.2016.511">Mignot et al [2016]</a> have recently identified potential additional <i>SYNGAP1</i> isoforms that could arise from alternative splicing.</p><p><b>Pathogenic variants.</b> The majority of pathogenic <i>SYNGAP1</i> variants are large deletions or heterozygous loss-of-function alleles such as nonsense and splice variants, frameshift insertions/deletions, and exon deletions; in addition, pathogenic heterozygous missense variants have been reported in a few instances (see review by <a class="bibr" href="#syngap1-id.REF.mignot.2016.511" rid="syngap1-id.REF.mignot.2016.511">Mignot et al [2016]</a>). Most pathogenic variants occur <i>de novo</i>.</p><p><b>Normal gene product.</b> The longest <i>SYNGAP1</i> isoform (NM_006772.2) encodes a protein of 1,343 amino acids that contains pleckstrin homology (PH), C2, RASGAP, SH3-binding, and coiled-coiled domains. Isoform 2 (NM_001130066.1) encodes a protein of 1,292 amino acids that contains the same domains as isoform 1 but has a different C-terminus that includes a QTRV motif required for postsynaptic scaffold protein interaction.</p><p><b>Abnormal gene product.</b>
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<i>SYNGAP1-</i>ID is caused by haploinsufficiency of SYNGAP1. Pathogenic variants include those likely to result in complete loss of SYNGAP1 protein expression as well as those predicted to cause truncated or misfolded nonfunctional SYNGAP1.</p></div><div id="syngap1-id.Chapter_Notes"><h2 id="_syngap1-id_Chapter_Notes_">Chapter Notes</h2><div id="syngap1-id.Revision_History"><h3>Revision History</h3><ul><li class="half_rhythm"><div>21 February 2019 (bp) Review posted live</div></li><li class="half_rhythm"><div>23 October 2017 (jm) Original submission</div></li></ul></div></div><div id="syngap1-id.References"><h2 id="_syngap1-id_References_">References</h2><div id="syngap1-id.Literature_Cited"><h3>Literature Cited</h3><ul class="simple-list"><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.berryer.2013.385">Berryer MH, Hamdan FF, Klitten LL, Møller RS, Carmant L, Schwartzentruber J, Patry L, Dobrzeniecka S, Rochefort D, Neugnot-Cerioli M, Lacaille JC, Niu Z, Eng CM, Yang Y, Palardy S, Belhumeur C, Rouleau GA, Tommerup N, Immken L, Beauchamp MH, Patel GS, Majewski J, Tarnopolsky MA, Scheffzek K, Hjalgrim H, Michaud JL, Di Cristo G. Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency. <span><span class="ref-journal">Hum Mutat. </span>2013;<span class="ref-vol">34</span>:385–94.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/23161826" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23161826</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.carvill.2013.825">Carvill GL, Heavin SB, Yendle SC, McMahon JM, O'Roak BJ, Cook J, Khan A, Dorschner MO, Weaver M, Calvert S, Malone S, Wallace G, Stanley T, Bye AM, Bleasel A, Howell KB, Kivity S, Mackay MT, Rodriguez-Casero V, Webster R, Korczyn A, Afawi Z, Zelnick N, Lerman-Sagie T, Lev D, Møller RS, Gill D, Andrade DM, Freeman JL, Sadleir LG, Shendure J, Berkovic SF, Scheffer IE, Mefford HC. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. <span><span class="ref-journal">Nat Genet. </span>2013;<span class="ref-vol">45</span>:825–30.</span> [<a href="/pmc/articles/PMC3704157/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC3704157</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/23708187" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23708187</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.de_ligt.2012.1921">de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, Kroes T, Vulto-van Silfhout AT, Koolen DA, de Vries P, Gilissen C, del Rosario M, Hoischen A, Scheffer H, de Vries BB, Brunner HG, Veltman JA, Vissers LE. Diagnostic exome sequencing in persons with severe intellectual disability. <span><span class="ref-journal">N Engl J Med. </span>2012;<span class="ref-vol">367</span>:1921–9.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/23033978" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23033978</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.fitzgerald.2015.223">Fitzgerald TW, Gerety SS, Jones WD, van Kogelenberg M, King DA, McRae J, Morley KI, Parthiban V, Al-Turki S, Ambridge K, Barrett DM, Bayzetinova T, Clayton S, Coomber EL, Gribble S, Jones P, Krishnappa N, Mason LE, et al. Large-scale discovery of novel genetic causes of developmental disorders. <span><span class="ref-journal">Nature. </span>2015;<span class="ref-vol">519</span>:223–8.</span> [<a href="/pmc/articles/PMC5955210/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5955210</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/25533962" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 25533962</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.hamdan.2011a.898">Hamdan FF, Daoud H, Piton A, Gauthier J, Dobrzeniecka S, Krebs MO, Joober R, Lacaille JC, Nadeau A, Milunsky JM, Wang Z, Carmant L, Mottron L, Beauchamp MH, Rouleau GA, Michaud JL. De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism. <span><span class="ref-journal">Biol Psychiatry. </span>2011a;<span class="ref-vol">69</span>:898–901.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/21237447" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21237447</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.hamdan.2011b.306">Hamdan FF, Gauthier J, Araki Y, Lin DT, Yoshizawa Y, Higashi K, Park AR, Spiegelman D, Dobrzeniecka S, Piton A, Tomitori H, Daoud H, Massicotte C, Henrion E, Diallo O, Shekarabi M, Marineau C, Shevell M, Maranda B, Mitchell G, Nadeau A, D'Anjou G, Vanasse M, Srour M, Lafrenière RG, Drapeau P, Lacaille JC, Kim E, Lee JR, Igarashi K, Huganir RL, Rouleau GA, Michaud JL, et al. Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability. <span><span class="ref-journal">Am J Hum Genet. </span>2011b;<span class="ref-vol">88</span>:306–16.</span> [<a href="/pmc/articles/PMC3059427/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC3059427</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/21376300" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21376300</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.hamdan.2009.599">Hamdan FF, Gauthier J, Spiegelman D, Noreau A, Yang Y, Pellerin S, Dobrzeniecka S, Côté M, Perreau-Linck E, Carmant L, D'Anjou G, Fombonne E, Addington AM, Rapoport JL, Delisi LE, Krebs MO, Mouaffak F, Joober R, Mottron L, Drapeau P, Marineau C, Lafrenière RG, Lacaille JC, Rouleau GA, Michaud JL, et al. Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation. <span><span class="ref-journal">N Engl J Med. </span>2009;<span class="ref-vol">360</span>:599–605.</span> [<a href="/pmc/articles/PMC2925262/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC2925262</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/19196676" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 19196676</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.klitten.2011.e190">Klitten LL, Møller RS, Nikanorova M, Silahtaroglu A, Hjalgrim H, Tommerup N. A balanced translocation disrupts SYNGAP1 in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA). <span><span class="ref-journal">Epilepsia. </span>2011;<span class="ref-vol">52</span>:e190–3.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/22050443" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 22050443</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.krepischi.2010.2376">Krepischi AC, Rosenberg C, Costa SS, Crolla JA, Huang S, Vianna-Morgante AM. A novel de novo microdeletion spanning the SYNGAP1 gene on the short arm of chromosome 6 associated with mental retardation. <span><span class="ref-journal">Am J Med Genet A. </span>2010;<span class="ref-vol">152A</span>:2376–8.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/20683986" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 20683986</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.mignot.2016.511">Mignot C, von Stülpnagel C, Nava C, Ville D, Sanlaville D, Lesca G, Rastetter A, Gachet B, Marie Y, Korenke GC, Borggraefe I, Hoffmann-Zacharska D, Szczepanik E, Rudzka-Dybała M, Yiş U, Çağlayan H, Isapof A, Marey I, Panagiotakaki E, Korff C, Rossier E, Riess A, Beck-Woedl S, Rauch A, Zweier C, Hoyer J, Reis A, Mironov M, Bobylova M, Mukhin K, Hernandez-Hernandez L, Maher B, Sisodiya S, Kuhn M, Glaeser D, Weckhuysen S, Myers CT, Mefford HC, Hörtnagel K, Biskup S, Lemke JR, Héron D, Kluger G, Depienne C, et al. Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy. <span><span class="ref-journal">J Med Genet. </span>2016;<span class="ref-vol">53</span>:511–22.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/26989088" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26989088</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.parker.2015.2231">Parker MJ, Fryer AE, Shears DJ, Lachlan KL, McKee SA, Magee AC, Mohammed S, Vasudevan PC, Park SM, Benoit V, Lederer D, Maystadt I, Study D, FitzPatrick DR. De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability. <span><span class="ref-journal">Am J Med Genet A. </span>2015;<span class="ref-vol">167A</span>:2231–7.</span> [<a href="/pmc/articles/PMC4744742/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4744742</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/26079862" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26079862</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.pinto.2010.368">Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, Cochrane L, Corsello C, Crawford EL, Crossett A, Cytrynbaum C, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Pilorge M, et al. Functional impact of global rare copy number variation in autism spectrum disorders. <span><span class="ref-journal">Nature. </span>2010;<span class="ref-vol">466</span>:368–72.</span> [<a href="/pmc/articles/PMC3021798/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC3021798</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/20531469" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 20531469</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.prchalova.2017.62">Prchalova D, Havlovicova M, Sterbova K, Stranecky V, Hancarova M, Sedlacek Z. Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype:case report. <span><span class="ref-journal">BMC Med Genet. </span>2017;<span class="ref-vol">18</span>:62.</span> [<a href="/pmc/articles/PMC5457574/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5457574</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/28576131" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28576131</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.rauch.2012.1674">Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, Joset P, Röpke A, Moog U, Riess A, Thiel CT, Tzschach A, Wiesener A, Wohlleber E, Zweier C, Ekici AB, Zink AM, Rump A, Meisinger C, Grallert H, Sticht H, Schenck A, Engels H, Rappold G, Schröck E, Wieacker P, Riess O, Meitinger T, Reis A, Strom TM. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. <span><span class="ref-journal">Lancet. </span>2012;<span class="ref-vol">380</span>:1674–82.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/23020937" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23020937</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.redin.2014.724">Redin C, Gérard B, Lauer J, Herenger Y, Muller J, Quartier A, Masurel-Paulet A, Willems M, Lesca G, El-Chehadeh S, Le Gras S, Vicaire S, Philipps M, Dumas M, Geoffroy V, Feger C, Haumesser N, Alembik Y, Barth M, Bonneau D, Colin E, Dollfus H, Doray B, Delrue MA, Drouin-Garraud V, Flori E, Fradin M, Francannet C, Goldenberg A, Lumbroso S, Mathieu-Dramard M, Martin-Coignard D, Lacombe D, Morin G, Polge A, Sukno S, Thauvin-Robinet C, Thevenon J, Doco-Fenzy M, Genevieve D, Sarda P, Edery P, Isidor B, Jost B, Olivier-Faivre L, Mandel JL, Piton A. Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing. <span><span class="ref-journal">J Med Genet. </span>2014;<span class="ref-vol">51</span>:724–36.</span> [<a href="/pmc/articles/PMC4215287/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4215287</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/25167861" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 25167861</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.richards.2015.405">Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. <span><span class="ref-journal">Genet Med. </span>2015;<span class="ref-vol">17</span>:405–24.</span> [<a href="/pmc/articles/PMC4544753/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4544753</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/25741868" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 25741868</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.vissers.2010.1109">Vissers LE, de Ligt J, Gilissen C, Janssen I, Steehouwer M, de Vries P, van Lier B, Arts P, Wieskamp N, del Rosario M, van Bon BW, Hoischen A, de Vries BB, Brunner HG, Veltman JA. A de novo paradigm for mental retardation. <span><span class="ref-journal">Nat Genet. </span>2010;<span class="ref-vol">42</span>:1109–12.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/21076407" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21076407</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.writzl.2013.1682">Writzl K, Knegt AC. 6p21.3 microdeletion involving the SYNGAP1 gene in a patient with intellectual disability, seizures, and severe speech impairment. <span><span class="ref-journal">Am J Med Genet A. </span>2013;<span class="ref-vol">161A</span>:1682–5.</span> [<a href="https://pubmed.ncbi.nlm.nih.gov/23687080" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23687080</span></a>]</div></p></li><li class="half_rhythm"><p><div class="bk_ref" id="syngap1-id.REF.zollino.2011.239">Zollino M, Gurrieri F, Orteschi D, Marangi G, Leuzzi V, Neri G. Integrated analysis of clinical signs and literature data for the diagnosis and therapy of a previously undescribed 6p21.3 deletion syndrome. <span><span class="ref-journal">Eur J Hum Genet. </span>2011;<span class="ref-vol">19</span>:239–42.</span> [<a href="/pmc/articles/PMC3025798/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC3025798</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/21119708" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21119708</span></a>]</div></p></li></ul></div></div><div id="bk_toc_contnr"></div></div></div><div class="fm-sec"><h2 id="_NBK537721_pubdet_">Publication Details</h2><h3>Author Information and Affiliations</h3><div class="contrib half_rhythm"><span itemprop="author">J Lloyd Holder, Jr</span>, MD, PhD<div class="affiliation small">Texas Children's Hospital<br />Houston, Texas<div><span class="email-label">Email: </span><a href="mailto:dev@null" data-email="ude.mcb@redloh" class="oemail">ude.mcb@redloh</a></div></div></div><div class="contrib half_rhythm"><span itemprop="author">Fadi F Hamdan</span>, PhD<div class="affiliation small">CHU Ste-Justine Research Center<br />Montreal, Quebec, Canada<div><span class="email-label">Email: </span><a href="mailto:dev@null" data-email="ac.cq.enitsuj-ets-ehcrehcer@nadmah.idaf" class="oemail">ac.cq.enitsuj-ets-ehcrehcer@nadmah.idaf</a></div></div></div><div class="contrib half_rhythm"><span itemprop="author">Jacques L Michaud</span>, MD<div class="affiliation small">CHU Ste-Justine Research Center<br />Montreal, Quebec, Canada<div><span class="email-label">Email: </span><a href="mailto:dev@null" data-email="ac.cq.enitsuj-ets-ehcrehcer@duahcim.seuqcaj" class="oemail">ac.cq.enitsuj-ets-ehcrehcer@duahcim.seuqcaj</a></div></div></div><h3>Publication History</h3><p class="small">Initial Posting: <span itemprop="datePublished">February 21, 2019</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>Holder JL Jr, Hamdan FF, Michaud JL. SYNGAP1-Related Intellectual Disability. 2019 Feb 21. 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/syne1ca-ar/?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/scs/?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="figobsyngap1idTmoleculargenetictestingu"><div id="syngap1-id.T.molecular_genetic_testing_u" class="table"><h3><span class="label">Table 1. </span></h3><div class="caption"><p>Molecular Genetic Testing Used in <i>SYNGAP1</i>-Related Intellectual Disability</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK537721/table/syngap1-id.T.molecular_genetic_testing_u/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__syngap1-id.T.molecular_genetic_testing_u_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_syngap1-id.T.molecular_genetic_testing_u_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_syngap1-id.T.molecular_genetic_testing_u_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Method</th><th id="hd_h_syngap1-id.T.molecular_genetic_testing_u_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Proportion of Probands with a Pathogenic Variant <sup>2</sup> Detectable by Method <sup>3</sup></th></tr></thead><tbody><tr><td headers="hd_h_syngap1-id.T.molecular_genetic_testing_u_1_1_1_1" rowspan="3" scope="row" colspan="1" style="text-align:left;vertical-align:middle;">
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<i>SYNGAP1</i>
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</td><td headers="hd_h_syngap1-id.T.molecular_genetic_testing_u_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Sequence analysis <sup>4</sup></td><td headers="hd_h_syngap1-id.T.molecular_genetic_testing_u_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">49/55 (89%)</td></tr><tr><td headers="hd_h_syngap1-id.T.molecular_genetic_testing_u_1_1_1_2" colspan="1" scope="row" rowspan="1" style="text-align:left;vertical-align:middle;">Gene-targeted deletion/duplication analysis <sup>5</sup></td><td headers="hd_h_syngap1-id.T.molecular_genetic_testing_u_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Unknown; see footnote 6.</td></tr><tr><td headers="hd_h_syngap1-id.T.molecular_genetic_testing_u_1_1_1_2" colspan="1" scope="row" rowspan="1" style="text-align:left;vertical-align:middle;">Chromosomal microarray analysis <sup>7</sup></td><td headers="hd_h_syngap1-id.T.molecular_genetic_testing_u_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">6/55 (11%)</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="syngap1-id.TF.1.1"><p class="no_margin">See <a href="/books/NBK537721/?report=reader#syngap1-id.molgen.TA">Table A. Genes and Databases</a> for chromosome locus and protein.</p></div></dd></dl><dl class="bkr_refwrap"><dt>2. </dt><dd><div id="syngap1-id.TF.1.2"><p class="no_margin">Based on a review of published series and case reports</p></div></dd></dl><dl class="bkr_refwrap"><dt>3. </dt><dd><div id="syngap1-id.TF.1.3"><p class="no_margin"><a class="bibr" href="#syngap1-id.REF.krepischi.2010.2376" rid="syngap1-id.REF.krepischi.2010.2376">Krepischi et al [2010]</a>, <a class="bibr" href="#syngap1-id.REF.pinto.2010.368" rid="syngap1-id.REF.pinto.2010.368">Pinto et al [2010]</a>, <a class="bibr" href="#syngap1-id.REF.vissers.2010.1109" rid="syngap1-id.REF.vissers.2010.1109">Vissers et al [2010]</a>, <a class="bibr" href="#syngap1-id.REF.hamdan.2011a.898" rid="syngap1-id.REF.hamdan.2011a.898">Hamdan et al [2011a]</a>, <a class="bibr" href="#syngap1-id.REF.hamdan.2011b.306" rid="syngap1-id.REF.hamdan.2011b.306">Hamdan et al [2011b]</a>, <a class="bibr" href="#syngap1-id.REF.klitten.2011.e190" rid="syngap1-id.REF.klitten.2011.e190">Klitten et al [2011]</a>, <a class="bibr" href="#syngap1-id.REF.zollino.2011.239" rid="syngap1-id.REF.zollino.2011.239">Zollino et al [2011]</a>, <a class="bibr" href="#syngap1-id.REF.de_ligt.2012.1921" rid="syngap1-id.REF.de_ligt.2012.1921">de Ligt et al [2012]</a>, <a class="bibr" href="#syngap1-id.REF.rauch.2012.1674" rid="syngap1-id.REF.rauch.2012.1674">Rauch et al [2012]</a>, <a class="bibr" href="#syngap1-id.REF.berryer.2013.385" rid="syngap1-id.REF.berryer.2013.385">Berryer et al [2013]</a>, <a class="bibr" href="#syngap1-id.REF.carvill.2013.825" rid="syngap1-id.REF.carvill.2013.825">Carvill et al [2013]</a>, <a class="bibr" href="#syngap1-id.REF.writzl.2013.1682" rid="syngap1-id.REF.writzl.2013.1682">Writzl & Knegt [2013]</a>, <a class="bibr" href="#syngap1-id.REF.redin.2014.724" rid="syngap1-id.REF.redin.2014.724">Redin et al [2014]</a>, <a class="bibr" href="#syngap1-id.REF.parker.2015.2231" rid="syngap1-id.REF.parker.2015.2231">Parker et al [2015]</a>, <a class="bibr" href="#syngap1-id.REF.mignot.2016.511" rid="syngap1-id.REF.mignot.2016.511">Mignot et al [2016]</a>, <a class="bibr" href="#syngap1-id.REF.prchalova.2017.62" rid="syngap1-id.REF.prchalova.2017.62">Prchalova et al [2017]</a></p></div></dd></dl><dl class="bkr_refwrap"><dt>4. </dt><dd><div id="syngap1-id.TF.1.4"><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>5. </dt><dd><div id="syngap1-id.TF.1.5"><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>6. </dt><dd><div id="syngap1-id.TF.1.6"><p class="no_margin">Gene-targeted methods will detect deletions of a single exon up to a whole gene; however, breakpoints of large deletions and/or deletion of adjacent genes may not be determined. If a whole-gene deletion is detected by a gene-targeted deletion/duplication assay, CMA is needed to determine the size of the deletion.</p></div></dd></dl><dl class="bkr_refwrap"><dt>7. </dt><dd><div id="syngap1-id.TF.1.7"><p class="no_margin">Chromosomal microarray analysis (CMA) using oligonucleotide arrays or SNP arrays. CMA designs in current clinical use target the 6p21.3 region; however, some 6p21.3 deletions may not have been detectable by older oligonucleotide or BAC platforms.</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobsyngap1idTrecommendedevaluationsfol"><div id="syngap1-id.T.recommended_evaluations_fol" class="table"><h3><span class="label">Table 2. </span></h3><div class="caption"><p>Recommended Evaluations Following Initial Diagnosis in Individuals with <i>SYNGAP1</i>-Related Intellectual Disability</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK537721/table/syngap1-id.T.recommended_evaluations_fol/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__syngap1-id.T.recommended_evaluations_fol_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">System/Concern</th><th id="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Evaluation</th><th id="hd_h_syngap1-id.T.recommended_evaluations_fol_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_syngap1-id.T.recommended_evaluations_fol_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
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<b>Eyes</b>
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</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">Ophthalmologic eval</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">Evidence of strabismus</td></tr><tr><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_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_syngap1-id.T.recommended_evaluations_fol_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Baseline eval for reflux &/or constipation; assessment for feeding problems</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Refer to gastroenterologist &/or feeding therapist for treatment if indicated.</td></tr><tr><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Musculoskeletal</b>
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</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Assessment for hip rotation/dysplasia, kyphoscoliosis, <i>pes planus</i></td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"></td></tr><tr><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_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_syngap1-id.T.recommended_evaluations_fol_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Neurologic eval</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Incl EEG & brain MRI if seizures are suspected</td></tr><tr><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Psychiatric/</b>
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<br />
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<b>Behavioral</b>
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</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Neuropsychiatric eval</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Screen persons age >12 mos for behavior concerns incl sleep disturbances, ADHD, anxiety, &/or traits suggestive of ASD.</td></tr><tr><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_1" rowspan="2" scope="row" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Miscellaneous/</b>
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<br />
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<b>Other</b>
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</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Developmental assessment</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Incl motor, speech/language eval, general cognitive, & vocational skills.</td></tr><tr><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_1_1_1_2" colspan="1" scope="col" rowspan="1" style="text-align:left;vertical-align:middle;">Consultation w/clinical geneticist &/or genetic counselor</td><td headers="hd_h_syngap1-id.T.recommended_evaluations_fol_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">ADHD = attention-deficit/hyperactivity disorder; ASD = autism spectrum disorder</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobsyngap1idTtreatmentofmanifestations"><div id="syngap1-id.T.treatment_of_manifestations" class="table"><h3><span class="label">Table 3. </span></h3><div class="caption"><p>Treatment of Manifestations in Individuals with <i>SYNGAP1</i>-Related Intellectual Disability</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK537721/table/syngap1-id.T.treatment_of_manifestations/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__syngap1-id.T.treatment_of_manifestations_lrgtbl__"><table class="no_bottom_margin"><thead><tr><th id="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_1" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">Manifestation/Concern</th><th id="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_2" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">Treatment</th><th id="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_3" scope="col" rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">Considerations/Other</th></tr></thead><tbody><tr><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Strabismus</b>
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</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Standard treatment(s) as recommended by ophthalmologist</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"></td></tr><tr><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Swallowing dysfunction</b>
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</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Nasogastric/gastrostomy feeding may be required for persistent feeding issues.</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"></td></tr><tr><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Constipation</b>
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</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Standard treatment as recommended by gastroenterologist</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Gastroenterology consultation, if severe</td></tr><tr><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
|
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<b>Hip rotation/dysplasia, kyphoscoliosis, & <i>pes planus</i></b>
|
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</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Standard treatment as recommended by orthopedist</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Orthopedic consultation may be considered.</td></tr><tr><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_1" scope="row" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">
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<b>Epilepsy</b>
|
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</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_2" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;">Standardized treatment w/ASMs by experienced neurologist</td><td headers="hd_h_syngap1-id.T.treatment_of_manifestations_1_1_1_3" rowspan="1" colspan="1" style="text-align:left;vertical-align:middle;"><ul><li class="half_rhythm"><div>To date, no guidelines on choice of specific ASMs</div></li><li class="half_rhythm"><div>Anecdotal reports of improved seizure control w/ketogenic diet in some persons</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">ASMs = anti-seizure medications</p></div></dd></dl></dl></div></div></div></article><article data-type="table-wrap" id="figobsyngap1idmolgenTA"><div id="syngap1-id.molgen.TA" class="table"><h3><span class="label">Table A.</span></h3><div class="caption"><p>SYNGAP1-Related Intellectual Disability: Genes and Databases</p></div><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK537721/table/syngap1-id.molgen.TA/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__syngap1-id.molgen.TA_lrgtbl__"><table class="no_bottom_margin"><tbody><tr><th id="hd_b_syngap1-id.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">Gene</th><th id="hd_b_syngap1-id.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">Chromosome Locus</th><th id="hd_b_syngap1-id.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">Protein</th><th id="hd_b_syngap1-id.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">Locus-Specific Databases</th><th id="hd_b_syngap1-id.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">HGMD</th><th id="hd_b_syngap1-id.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">ClinVar</th></tr><tr><td headers="hd_b_syngap1-id.molgen.TA_1_1_1_1" rowspan="1" colspan="1" style="vertical-align:top;">
|
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<a href="/gene/8831" ref="pagearea=body&targetsite=entrez&targetcat=link&targettype=gene">
|
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<i>SYNGAP1</i>
|
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</a>
|
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</td><td headers="hd_b_syngap1-id.molgen.TA_1_1_1_2" rowspan="1" colspan="1" style="vertical-align:top;">
|
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<a href="https://www.ncbi.nlm.nih.gov/genome/gdv/?context=gene&acc=8831" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">6p21<wbr style="display:inline-block"></wbr>​.32</a>
|
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</td><td headers="hd_b_syngap1-id.molgen.TA_1_1_1_3" rowspan="1" colspan="1" style="vertical-align:top;">
|
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<a href="http://www.uniprot.org/uniprot/Q96PV0" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Ras/Rap GTPase-activating protein SynGAP</a>
|
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</td><td headers="hd_b_syngap1-id.molgen.TA_1_1_1_4" rowspan="1" colspan="1" style="vertical-align:top;">
|
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<a href="https://lovd.nl/SYNGAP1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">SYNGAP1 database</a>
|
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</td><td headers="hd_b_syngap1-id.molgen.TA_1_1_1_5" rowspan="1" colspan="1" style="vertical-align:top;">
|
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<a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=SYNGAP1" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">SYNGAP1</a>
|
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</td><td headers="hd_b_syngap1-id.molgen.TA_1_1_1_6" rowspan="1" colspan="1" style="vertical-align:top;">
|
|
<a href="https://www.ncbi.nlm.nih.gov/clinvar/?term=SYNGAP1[gene]" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">SYNGAP1</a>
|
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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 id="syngap1-id.TFA.1"><p class="no_margin">Data are compiled from the following standard references: gene from
|
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<a href="http://www.genenames.org/index.html" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">HGNC</a>;
|
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chromosome locus from
|
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<a href="http://www.omim.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">OMIM</a>;
|
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protein from <a href="http://www.uniprot.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">UniProt</a>.
|
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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="figobsyngap1idmolgenTB"><div id="syngap1-id.molgen.TB" class="table"><h3><span class="label">Table B.</span></h3><div class="caption"><p>OMIM Entries for SYNGAP1-Related Intellectual Disability (<a href="/omim/603384,612621" 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/NBK537721/table/syngap1-id.molgen.TB/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__syngap1-id.molgen.TB_lrgtbl__"><table><tbody><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
|
<a href="/omim/603384" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">603384</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">SYNAPTIC RAS-GTPase-ACTIVATING PROTEIN 1; SYNGAP1</td></tr><tr><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">
|
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<a href="/omim/612621" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=omim">612621</a></td><td rowspan="1" colspan="1" style="text-align:left;vertical-align:top;">INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5</td></tr></tbody></table></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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