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<meta name="keywords" content="C1861329, anatomical abnormality, finding, narrow spinal canal, spinal canal stenosis, spinal stenosis, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="An abnormal narrowing of the spinal canal." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
UID=396107
ConceptID=C1861329
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Spinal canal stenosis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>396107</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C1861329</a></dd><dt><span class="dotprefix"></span></dt><dd>Anatomical Abnormality; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
<td>Spinal stenosis</td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0003416">HP:0003416</a></td></tr>
<tr><td>Monarch Initiative:</td>
<td><a href="https://monarchinitiative.org/disease/MONDO:0005965" target="_blank">MONDO:0005965</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln">An abnormal narrowing of the spinal canal. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
</div>
<div class="portlet mgSection" id="ID_118">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test,  </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test,  </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM,  </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>,  </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar  </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1861329[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=396107">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Spinal canal stenosis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/1763488" ref="tree=MeSH" title="MedGen record for Abnormality of the musculoskeletal system">Abnormality of the musculoskeletal system</a></span><ul><li><span class="TLline"><a href="/medgen/867418" ref="tree=MeSH" title="MedGen record for Abnormality of the skeletal system">Abnormality of the skeletal system</a></span><ul><li><span class="TLline"><a href="/medgen/868760" ref="tree=MeSH" title="MedGen record for Abnormal skeletal morphology">Abnormal skeletal morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892434" ref="tree=MeSH" title="MedGen record for Abnormal axial skeleton morphology">Abnormal axial skeleton morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892426" ref="tree=MeSH" title="MedGen record for Abnormality of the vertebral column">Abnormality of the vertebral column</a></span><ul><li><span class="matched_ds">Spinal canal stenosis</span><ul><li><span class="TLline"><a href="/medgen/335056" ref="tree=MeSH" title="MedGen record for Cervical spinal canal stenosis">Cervical spinal canal stenosis</a></span></li><li><span class="TLline"><a href="/medgen/488791" ref="tree=MeSH" title="MedGen record for Lumbar spinal canal stenosis">Lumbar spinal canal stenosis</a></span></li><li><span class="TLline"><a href="/medgen/867265" ref="tree=MeSH" title="MedGen record for Spinal stenosis with reduced interpedicular distance">Spinal stenosis with reduced interpedicular distance</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
</div>
<div class="portlet mgSection" id="ID_112">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln clinfeat">
<div class="divPopper rprt" id="rdis_39008"><div><strong>Proteus syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>39008</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C0085261</a></dd><dt><span class="dotprefix"></span></dt><dd>Neoplastic Process</dd></dl></div></div></div>
<div class="spaceAbove">Proteus syndrome (PS) is characterized by progressive segmental or patchy overgrowth most commonly affecting the skeleton, skin, adipose, and central nervous systems. In most individuals PS has modest or no manifestations at birth, develops and progresses rapidly beginning in the toddler period, and relentlessly progresses through childhood, causing severe overgrowth and disfigurement. It is associated with a range of tumors, pulmonary complications, and a striking predisposition to deep vein thrombosis and pulmonary embolism.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/39008">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_90977"><div><strong>Symphalangism-brachydactyly syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>90977</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C0342282</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Multiple synostoses syndrome is characterized by multiple joint fusions, usually commencing in the hands, conductive deafness, and characteristic facial features, including a broad, tubular-shaped nose and a thin upper vermilion. Other features include brachydactyly, hypoplastic or absent middle phalanges, radial head dislocation, and pectus carinatum (summary by Takahashi et al., 2001).&#13; Genetic Heterogeneity of Multiple Synostoses Syndrome&#13; Other forms of multiple synostoses syndrome include SYNS2 (610017), caused by mutation in the GDF5 gene (601146) on chromosome 20q11; SYNS3 (612961), caused by mutation in the FGF9 gene (600921) on chromosome 13q12; and SYNS4 (617898), caused by mutation in the GDF6 gene (601147) on chromosome 8q22.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/90977">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_196551"><div><strong>Familial X-linked hypophosphatemic vitamin D refractory rickets</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>196551</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C0733682</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">The phenotypic spectrum of X-linked hypophosphatemia (XLH) ranges from isolated hypophosphatemia to severe lower extremity bowing and/or craniosynostosis, usually involving the sagittal suture with consequent scaphocephaly. XLH typically manifests in the first two years of life with lower extremity bowing due to the onset of weight-bearing; however, it sometimes does not manifest until adulthood, as previously unevaluated short stature. Adults may present with calcification of the tendons, ligaments, and joint capsules, joint pain, fatigue, insufficiency fractures, and impaired mobility. Persons with XLH are prone to spontaneous dental abscesses; sensorineural hearing loss has also been reported. Rarely, individuals with XLH can suffer from spinal stenosis, Chiari I malformation, syringomyelia, and/or raised intracranial pressure.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/196551">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_358388"><div><strong>Weill-Marchesani syndrome 2, dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>358388</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C1869115</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterized by abnormalities of the lens of the eye, short stature, brachydactyly, joint stiffness, and cardiovascular defects. The ocular problems, typically recognized in childhood, include microspherophakia (small spherical lens), myopia secondary to the abnormal shape of the lens, ectopia lentis (abnormal position of the lens), and glaucoma, which can lead to blindness. Height of adult males is 142-169 cm; height of adult females is 130-157 cm. Autosomal recessive WMS cannot be distinguished from autosomal dominant WMS by clinical findings alone.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/358388">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_477858"><div><strong>Acrodysostosis 1 with or without hormone resistance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>477858</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C3276228</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Acrodysostosis-1 (ACRDYS1) is a form of skeletal dysplasia characterized by short stature, severe brachydactyly, facial dysostosis, and nasal hypoplasia. Affected individuals often have advanced bone age and obesity. Laboratory studies show resistance to multiple hormones, including parathyroid, thyrotropin, calcitonin, growth hormone-releasing hormone, and gonadotropin (summary by Linglart et al., 2011). However, not all patients show endocrine abnormalities (Lee et al., 2012).&#13; Genetic Heterogeneity of Acrodysostosis&#13; See also ACRDYS2 (614613), caused by mutation in the PDE4D gene (600129) on chromosome 5q12.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/477858">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_766164"><div><strong>Acrodysostosis 2 with or without hormone resistance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766164</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C3553250</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Acrodysostosis-2 (ACRDYS2) is a rare skeletal dysplasia characterized by brachydactyly, facial dysostosis, and spinal stenosis. Many patients have intellectual disability and some have hormone resistance (summary by Michot et al., 2012 and Lee et al., 2012).&#13; For a discussion of genetic heterogeneity of acrodysostosis, see ACRDYS1 (101800).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/766164">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_863379"><div><strong>Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>863379</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C4014942</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">CAGSSS, which comprises cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia, is an autosomal recessive multisystemic disorder with a highly variable phenotypic spectrum. Not all of these features are always present, and almost all the features may present at different times and/or become more apparent with age. The skeletal features are consistent with spondyloepimetaphyseal dysplasia (SEMD) (summary by Vona et al., 2018).&#13; One family had a distinctive presentation with infantile-onset intractable seizures and cortical abnormalities reminiscent of Leigh syndrome (see 256000). The correlation between genotype and phenotype remains unclear, but since the IARS2 gene is involved in mitochondrial function, heterogeneous manifestations can be expected (Takezawa et al., 2018).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/863379">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_899713"><div><strong>Spondylocostal dysostosis 6, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>899713</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C4225279</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Spondylocostal dysostosis (SCDO), defined radiographically as multiple segmentation defects of the vertebrae in combination with abnormalities of the ribs, is characterized clinically by a short trunk in proportion to height; short neck; and non-progressive mild scoliosis in most affected individuals rarely, more significant scoliosis occurs. Respiratory function in neonates with severe disease may be compromised by reduced size of the thorax. By age two years lung growth may improve sufficiently to support relatively normal growth and development. In severely affected individuals with restricted pulmonary capacity, there is a possibility that pulmonary hypertension may eventually impact cardiac function. Males with SCDO appear to be at increased risk for inguinal hernia.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/899713">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1637058"><div><strong>Weill-Marchesani syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1637058</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C4552002</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterized by abnormalities of the lens of the eye, short stature, brachydactyly, joint stiffness, and cardiovascular defects. The ocular problems, typically recognized in childhood, include microspherophakia (small spherical lens), myopia secondary to the abnormal shape of the lens, ectopia lentis (abnormal position of the lens), and glaucoma, which can lead to blindness. Height of adult males is 142-169 cm; height of adult females is 130-157 cm. Autosomal recessive WMS cannot be distinguished from autosomal dominant WMS by clinical findings alone.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1637058">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1648483"><div><strong>Hyper-IgE recurrent infection syndrome 3, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1648483</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C4748969</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Hyper-IgE syndrome-3 with recurrent infections (HIES3) is an autosomal recessive immunologic disorder characterized by childhood onset of atopic dermatitis, skin infections particularly with Staphylococcus aureus, recurrent sinopulmonary infections, and increased serum IgE and IgG. Patients are susceptible to bacterial and fungal infections, including chronic mucocutaneous candidiasis. Immunologic workup shows impaired differentiation of CD4+ T cells into T-helper 17 cells, decreased memory B cells, and often decreased NK cells (summary by Beziat et al., 2018).&#13; For a discussion of genetic heterogeneity of hyper-IgE syndrome, see HIES1 (147060).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1648483">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1684730"><div><strong>Noonan syndrome 12</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684730</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C5231432</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Noonan syndrome (NS) is characterized by characteristic facies, short stature, congenital heart defect, and developmental delay of variable degree. Other findings can include broad or webbed neck, unusual chest shape with superior pectus carinatum and inferior pectus excavatum, cryptorchidism, varied coagulation defects, lymphatic dysplasias, and ocular abnormalities. Although birth length is usually normal, final adult height approaches the lower limit of normal. Congenital heart disease occurs in 50%-80% of individuals. Pulmonary valve stenosis, often with dysplasia, is the most common heart defect and is found in 20%-50% of individuals. Hypertrophic cardiomyopathy, found in 20%-30% of individuals, may be present at birth or develop in infancy or childhood. Other structural defects include atrial and ventricular septal defects, branch pulmonary artery stenosis, and tetralogy of Fallot. Up to one fourth of affected individuals have mild intellectual disability, and language impairments in general are more common in NS than in the general population.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1684730">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1854940"><div><strong>Intellectual developmental disorder, x-linked, syndromic 37</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1854940</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C5935567</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">X-linked syndromic intellectual developmental disorder-37 (MRXS37) is a developmental disorder showing phenotypic variability and variable severity. Male mutation carriers tend to be more severely affected than female mutation carriers, some of whom may even be asymptomatic. In general, the disorder is characterized by global developmental delay with delayed walking, speech delay, impaired intellectual development that ranges from borderline low to moderate, and behavioral abnormalities, such as autism and sleeping difficulties. Many patients are able to attend mainstream schools with assistance and work under supervision. Additional more variable features include sensorineural hearing loss, ocular anomalies, feeding difficulties, dysmorphic facial features, inguinal and umbilical hernia, genitourinary defects, congenital heart defects, musculoskeletal anomalies, and endocrine dysfunction, such as hypogonadism or hyperparathyroidism (Shepherdson et al., 2024).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1854940">Condition Record</a></div></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_477858" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acrodysostosis 1 with or without hormone resistance</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766164" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acrodysostosis 2 with or without hormone resistance</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_863379" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_196551" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Familial X-linked hypophosphatemic vitamin D refractory rickets</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1648483" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hyper-IgE recurrent infection syndrome 3, autosomal recessive</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (12)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1854940" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual developmental disorder, x-linked, syndromic 37</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684730" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Noonan syndrome 12</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_39008" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Proteus syndrome</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_899713" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondylocostal dysostosis 6, autosomal recessive</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_90977" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Symphalangism-brachydactyly syndrome</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1637058" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Weill-Marchesani syndrome 1</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_358388" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Weill-Marchesani syndrome 2, dominant</a></div></span></div></div>
</div>
<div class="portlet mgSection" id="ID_105">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
<div class="nl"><a target="_blank" href="/pubmed/34070375">Advantages and Disadvantages of Different Treatment Methods in Achondroplasia: A Review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Wrobel W,
Pach E,
Ben-Skowronek I</span><br />
<span class="medgenPMjournal">Int J Mol Sci</span>
2021 May 25;22(11)
doi: 10.3390/ijms22115573.
<span class="bold">PMID: </span><a href="/pubmed/34070375" target="_blank">34070375</a><a href="/pmc/articles/PMC8197470" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25612248">Prostaglandin E1 Treatment for Lumbar Spinal Canal Stenosis: Review of the Literature.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yoshihara H</span><br />
<span class="medgenPMjournal">Pain Pract</span>
2016 Feb;16(2):245-56.
Epub 2015 Jan 7
doi: 10.1111/papr.12272.
<span class="bold">PMID: </span><a href="/pubmed/25612248" target="_blank">25612248</a></div>
<div class="nl"><a target="_blank" href="/pubmed/18026865">Diagnosis and conservative management of degenerative lumbar spondylolisthesis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kalichman L,
Hunter DJ</span><br />
<span class="medgenPMjournal">Eur Spine J</span>
2008 Mar;17(3):327-335.
Epub 2007 Nov 17
doi: 10.1007/s00586-007-0543-3.
<span class="bold">PMID: </span><a href="/pubmed/18026865" target="_blank">18026865</a><a href="/pmc/articles/PMC2270383" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22spinal%20canal%20stenosis%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (26)</a></div></div>
</div>
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
<div class="portlet mgSection" id="ID_103">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
<div class="nl"><a target="_blank" href="/pubmed/38569854">Promising horizons in achondroplasia along with the development of new drugs.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Ozono K,
Kubota T,
Michigami T</span><br />
<span class="medgenPMjournal">Endocr J</span>
2024 Jul 12;71(7):643-650.
Epub 2024 Apr 4
doi: 10.1507/endocrj.EJ24-0109.
<span class="bold">PMID: </span><a href="/pubmed/38569854" target="_blank">38569854</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28232045">Multiple levels of spinal canal stenosis in endemic skeletal fluorosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Zhu C,
Zhou S,
Liu L,
Song Y</span><br />
<span class="medgenPMjournal">Joint Bone Spine</span>
2017 Dec;84(6):737.
Epub 2017 Feb 14
doi: 10.1016/j.jbspin.2017.01.009.
<span class="bold">PMID: </span><a href="/pubmed/28232045" target="_blank">28232045</a></div>
<div class="nl"><a target="_blank" href="/pubmed/27544679">Lumbar scoliosis associated with spinal stenosis in idiopathic and degenerative cases.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Le Huec JC,
Cogniet A,
Mazas S,
Faundez A</span><br />
<span class="medgenPMjournal">Eur J Orthop Surg Traumatol</span>
2016 Oct;26(7):705-12.
Epub 2016 Aug 20
doi: 10.1007/s00590-016-1829-0.
<span class="bold">PMID: </span><a href="/pubmed/27544679" target="_blank">27544679</a></div>
<div class="nl"><a target="_blank" href="/pubmed/16833245">Laminectomy for thoracic spinal canal stenosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kalfas IH</span><br />
<span class="medgenPMjournal">Neurosurg Focus</span>
2000 Oct 15;9(4):e2.
doi: 10.3171/foc.2000.9.4.3.
<span class="bold">PMID: </span><a href="/pubmed/16833245" target="_blank">16833245</a></div>
<div class="nl"><a target="_blank" href="/pubmed/2769282">Developmental spinal canal stenosis and somatotype.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Nightingale S</span><br />
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
1989 Jul;52(7):887-90.
doi: 10.1136/jnnp.52.7.887.
<span class="bold">PMID: </span><a href="/pubmed/2769282" target="_blank">2769282</a><a href="/pmc/articles/PMC1031938" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Spinal%20canal%20stenosis%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (519)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/38909909">Deep learning-based detection of lumbar spinal canal stenosis using convolutional neural networks.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Suzuki H,
Kokabu T,
Yamada K,
Ishikawa Y,
Yabu A,
Yanagihashi Y,
Hyakumachi T,
Tachi H,
Shimizu T,
Endo T,
Ohnishi T,
Ukeba D,
Nagahama K,
Takahata M,
Sudo H,
Iwasaki N</span><br />
<span class="medgenPMjournal">Spine J</span>
2024 Nov;24(11):2086-2101.
Epub 2024 Jun 22
doi: 10.1016/j.spinee.2024.06.009.
<span class="bold">PMID: </span><a href="/pubmed/38909909" target="_blank">38909909</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34904218">Lumbar spinal canal stenosis: An early sign of amyloid transthyretin related amyloidosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Graziani A,
Cenni P,
Lisi M,
Domenicali M,
Graziani L</span><br />
<span class="medgenPMjournal">Kardiol Pol</span>
2022;80(2):218-219.
Epub 2021 Dec 14
doi: 10.33963/KP.a2021.0179.
<span class="bold">PMID: </span><a href="/pubmed/34904218" target="_blank">34904218</a></div>
<div class="nl"><a target="_blank" href="/pubmed/18026865">Diagnosis and conservative management of degenerative lumbar spondylolisthesis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kalichman L,
Hunter DJ</span><br />
<span class="medgenPMjournal">Eur Spine J</span>
2008 Mar;17(3):327-335.
Epub 2007 Nov 17
doi: 10.1007/s00586-007-0543-3.
<span class="bold">PMID: </span><a href="/pubmed/18026865" target="_blank">18026865</a><a href="/pmc/articles/PMC2270383" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/12952026">Spinal canal stenosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tan SB</span><br />
<span class="medgenPMjournal">Singapore Med J</span>
2003 Apr;44(4):168-9.
<span class="bold">PMID: </span><a href="/pubmed/12952026" target="_blank">12952026</a></div>
<div class="nl"><a target="_blank" href="/pubmed/16833245">Laminectomy for thoracic spinal canal stenosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kalfas IH</span><br />
<span class="medgenPMjournal">Neurosurg Focus</span>
2000 Oct 15;9(4):e2.
doi: 10.3171/foc.2000.9.4.3.
<span class="bold">PMID: </span><a href="/pubmed/16833245" target="_blank">16833245</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Spinal%20canal%20stenosis%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (381)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/34070375">Advantages and Disadvantages of Different Treatment Methods in Achondroplasia: A Review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Wrobel W,
Pach E,
Ben-Skowronek I</span><br />
<span class="medgenPMjournal">Int J Mol Sci</span>
2021 May 25;22(11)
doi: 10.3390/ijms22115573.
<span class="bold">PMID: </span><a href="/pubmed/34070375" target="_blank">34070375</a><a href="/pmc/articles/PMC8197470" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28232045">Multiple levels of spinal canal stenosis in endemic skeletal fluorosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Zhu C,
Zhou S,
Liu L,
Song Y</span><br />
<span class="medgenPMjournal">Joint Bone Spine</span>
2017 Dec;84(6):737.
Epub 2017 Feb 14
doi: 10.1016/j.jbspin.2017.01.009.
<span class="bold">PMID: </span><a href="/pubmed/28232045" target="_blank">28232045</a></div>
<div class="nl"><a target="_blank" href="/pubmed/27544679">Lumbar scoliosis associated with spinal stenosis in idiopathic and degenerative cases.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Le Huec JC,
Cogniet A,
Mazas S,
Faundez A</span><br />
<span class="medgenPMjournal">Eur J Orthop Surg Traumatol</span>
2016 Oct;26(7):705-12.
Epub 2016 Aug 20
doi: 10.1007/s00590-016-1829-0.
<span class="bold">PMID: </span><a href="/pubmed/27544679" target="_blank">27544679</a></div>
<div class="nl"><a target="_blank" href="/pubmed/18026865">Diagnosis and conservative management of degenerative lumbar spondylolisthesis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kalichman L,
Hunter DJ</span><br />
<span class="medgenPMjournal">Eur Spine J</span>
2008 Mar;17(3):327-335.
Epub 2007 Nov 17
doi: 10.1007/s00586-007-0543-3.
<span class="bold">PMID: </span><a href="/pubmed/18026865" target="_blank">18026865</a><a href="/pmc/articles/PMC2270383" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/17209669">Limaprost.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Swainston Harrison T,
Plosker GL</span><br />
<span class="medgenPMjournal">Drugs</span>
2007;67(1):109-18; discussion 119-20.
doi: 10.2165/00003495-200767010-00010.
<span class="bold">PMID: </span><a href="/pubmed/17209669" target="_blank">17209669</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Spinal%20canal%20stenosis%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (212)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/38909909">Deep learning-based detection of lumbar spinal canal stenosis using convolutional neural networks.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Suzuki H,
Kokabu T,
Yamada K,
Ishikawa Y,
Yabu A,
Yanagihashi Y,
Hyakumachi T,
Tachi H,
Shimizu T,
Endo T,
Ohnishi T,
Ukeba D,
Nagahama K,
Takahata M,
Sudo H,
Iwasaki N</span><br />
<span class="medgenPMjournal">Spine J</span>
2024 Nov;24(11):2086-2101.
Epub 2024 Jun 22
doi: 10.1016/j.spinee.2024.06.009.
<span class="bold">PMID: </span><a href="/pubmed/38909909" target="_blank">38909909</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30953182">Carpal tunnel syndrome and spinal canal stenosis: harbingers of transthyretin amyloid cardiomyopathy?</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Aus dem Siepen F,
Hein S,
Prestel S,
Baumgärtner C,
Schönland S,
Hegenbart U,
Röcken C,
Katus HA,
Kristen AV</span><br />
<span class="medgenPMjournal">Clin Res Cardiol</span>
2019 Dec;108(12):1324-1330.
Epub 2019 Apr 5
doi: 10.1007/s00392-019-01467-1.
<span class="bold">PMID: </span><a href="/pubmed/30953182" target="_blank">30953182</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28232045">Multiple levels of spinal canal stenosis in endemic skeletal fluorosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Zhu C,
Zhou S,
Liu L,
Song Y</span><br />
<span class="medgenPMjournal">Joint Bone Spine</span>
2017 Dec;84(6):737.
Epub 2017 Feb 14
doi: 10.1016/j.jbspin.2017.01.009.
<span class="bold">PMID: </span><a href="/pubmed/28232045" target="_blank">28232045</a></div>
<div class="nl"><a target="_blank" href="/pubmed/18026865">Diagnosis and conservative management of degenerative lumbar spondylolisthesis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kalichman L,
Hunter DJ</span><br />
<span class="medgenPMjournal">Eur Spine J</span>
2008 Mar;17(3):327-335.
Epub 2007 Nov 17
doi: 10.1007/s00586-007-0543-3.
<span class="bold">PMID: </span><a href="/pubmed/18026865" target="_blank">18026865</a><a href="/pmc/articles/PMC2270383" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/3631079">Mortality in achondroplasia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hecht JT,
Francomano CA,
Horton WA,
Annegers JF</span><br />
<span class="medgenPMjournal">Am J Hum Genet</span>
1987 Sep;41(3):454-64.
<span class="bold">PMID: </span><a href="/pubmed/3631079" target="_blank">3631079</a><a href="/pmc/articles/PMC1684180" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Spinal%20canal%20stenosis%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (230)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/38909909">Deep learning-based detection of lumbar spinal canal stenosis using convolutional neural networks.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Suzuki H,
Kokabu T,
Yamada K,
Ishikawa Y,
Yabu A,
Yanagihashi Y,
Hyakumachi T,
Tachi H,
Shimizu T,
Endo T,
Ohnishi T,
Ukeba D,
Nagahama K,
Takahata M,
Sudo H,
Iwasaki N</span><br />
<span class="medgenPMjournal">Spine J</span>
2024 Nov;24(11):2086-2101.
Epub 2024 Jun 22
doi: 10.1016/j.spinee.2024.06.009.
<span class="bold">PMID: </span><a href="/pubmed/38909909" target="_blank">38909909</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35979579">Cauda equina movement during the Valsalva maneuver in two patients with Lumbar spinal canal stenosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yamakuni R,
Ishikawa H,
Hasegawa O,
Sekino H,
Ishii S,
Otani K,
Ito H</span><br />
<span class="medgenPMjournal">Fukushima J Med Sci</span>
2022;68(2):135-141.
doi: 10.5387/fms.2022-12.
<span class="bold">PMID: </span><a href="/pubmed/35979579" target="_blank">35979579</a><a href="/pmc/articles/PMC9493334" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25612248">Prostaglandin E1 Treatment for Lumbar Spinal Canal Stenosis: Review of the Literature.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yoshihara H</span><br />
<span class="medgenPMjournal">Pain Pract</span>
2016 Feb;16(2):245-56.
Epub 2015 Jan 7
doi: 10.1111/papr.12272.
<span class="bold">PMID: </span><a href="/pubmed/25612248" target="_blank">25612248</a></div>
<div class="nl"><a target="_blank" href="/pubmed/1462211">Hypertrophied ligamentum flavum in lumbar spinal canal stenosis. Pathogenesis and morphologic and immunohistochemical observation.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yoshida M,
Shima K,
Taniguchi Y,
Tamaki T,
Tanaka T</span><br />
<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
1992 Nov;17(11):1353-60.
doi: 10.1097/00007632-199211000-00015.
<span class="bold">PMID: </span><a href="/pubmed/1462211" target="_blank">1462211</a></div>
<div class="nl"><a target="_blank" href="/pubmed/1797731">Achondroplasia and lumbar spinal stenosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Savini R,
Gargiulo G,
Cervellati S,
Di Silvestre M</span><br />
<span class="medgenPMjournal">Ital J Orthop Traumatol</span>
1991 Jun;17(2):199-209.
<span class="bold">PMID: </span><a href="/pubmed/1797731" target="_blank">1797731</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Spinal%20canal%20stenosis%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (395)</a></div></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="nl"><a target="_blank" href="/pubmed/37625633">Risk Factors for Cerebrospinal Fluid Leakage After Extradural Spine Surgery: A Meta-Analysis and Systematic Review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Jin JY,
Yu M,
Xu RF,
Sun Y,
Li BH,
Zhou FF</span><br />
<span class="medgenPMjournal">World Neurosurg</span>
2023 Nov;179:e269-e280.
Epub 2023 Aug 23
doi: 10.1016/j.wneu.2023.08.075.
<span class="bold">PMID: </span><a href="/pubmed/37625633" target="_blank">37625633</a></div>
<div class="nl"><a target="_blank" href="/pubmed/36396060">Meta-Analysis of Simultaneous versus Staged Decompression of Stenotic Regions in Patients with Tandem Spinal Stenosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lu C,
Qiu H,
Huang X,
Yang X,
Liu D,
Zhang S,
Zhang Y</span><br />
<span class="medgenPMjournal">World Neurosurg</span>
2023 Feb;170:e441-e454.
Epub 2022 Nov 14
doi: 10.1016/j.wneu.2022.11.028.
<span class="bold">PMID: </span><a href="/pubmed/36396060" target="_blank">36396060</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35871273">Efficacy and safety of epidural anesthesia versus local anesthesia in percutaneous transforaminal endoscopic discectomy: a systematic review and meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Zheng B,
Guo C,
Xu S,
Jin L,
Hong Y,
Liu C,
Liu H</span><br />
<span class="medgenPMjournal">Ann Palliat Med</span>
2022 Aug;11(8):2676-2684.
Epub 2022 Jul 11
doi: 10.21037/apm-21-3413.
<span class="bold">PMID: </span><a href="/pubmed/35871273" target="_blank">35871273</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34474449">Intraoperative Ultrasound in Spine Decompression Surgery: A Systematic Review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tat J,
Tat J,
Yoon S,
Yee AJM,
Larouche J</span><br />
<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
2022 Jan 15;47(2):E73-E85.
doi: 10.1097/BRS.0000000000004111.
<span class="bold">PMID: </span><a href="/pubmed/34474449" target="_blank">34474449</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26363561">Surgery for adult spondylolisthesis: a systematic review of the evidence.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schulte TL,
Ringel F,
Quante M,
Eicker SO,
Muche-Borowski C,
Kothe R</span><br />
<span class="medgenPMjournal">Eur Spine J</span>
2016 Aug;25(8):2359-67.
Epub 2015 Sep 12
doi: 10.1007/s00586-015-4177-6.
<span class="bold">PMID: </span><a href="/pubmed/26363561" target="_blank">26363561</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Spinal%20canal%20stenosis%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (11)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C1861329%5bDISCUI%5d&amp;filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (6)</a></li>
<li><a href="/gtr/tests?term=C1861329%5bDISCUI%5d&amp;filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (6)</a></li>
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C1861329%5bDISCUI%5d" target="_blank">See all (6)</a></total></li>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Spinal%20canal%20stenosis" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22spinal%20canal%20stenosis%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Spinal%20canal%20stenosis%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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