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<meta name="keywords" content="C0205700, ash, asymmetric septal hypertrophy, disease or syndrome, 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="Hypertrophic cardiomyopathy with an asymmetrical pattern of hypertrophy, with a predilection for the interventricular septum and myocyte disarray." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
UID=104705
ConceptID=C0205700
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Asymmetric septal hypertrophy<span class="h1sub">(ASH)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>104705</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.">C0205700</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
<td>ASH; ASYMMETRIC SEPTAL HYPERTROPHY</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:0001670">HP:0001670</a></td></tr>
<tr><td>OMIM<span class="superscript">®</span>:</td>
<td><a href="https://omim.org/entry/192600" target="_blank">192600</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">Hypertrophic cardiomyopathy with an asymmetrical pattern of hypertrophy, with a predilection for the interventricular septum and myocyte disarray. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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<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 unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=104705" target="_blank" href="/omim/192600">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=104705" ref="ncbi_uid=104705">V</a></span></span><span class="TLline">Asymmetric septal hypertrophy</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/116727" ref="tree=MeSH" title="MedGen record for Abnormality of the cardiovascular system">Abnormality of the cardiovascular system</a></span><ul><li><span class="TLline"><a href="/medgen/892473" ref="tree=MeSH" title="MedGen record for Abnormal cardiovascular system morphology">Abnormal cardiovascular system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/6748" ref="tree=MeSH" title="MedGen record for Abnormal heart morphology">Abnormal heart morphology</a></span><ul><li><span class="TLline"><a href="/medgen/871271" ref="tree=MeSH" title="MedGen record for Abnormal myocardium morphology">Abnormal myocardium morphology</a></span><ul><li><span class="TLline"><a href="/medgen/209232" ref="tree=MeSH" title="MedGen record for Cardiomyopathy">Cardiomyopathy</a></span><ul><li><span class="TLline"><a href="/medgen/2881" ref="tree=MeSH" title="MedGen record for Hypertrophic cardiomyopathy">Hypertrophic cardiomyopathy</a></span><ul><li><span class="matched_ds">Asymmetric septal hypertrophy</span></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_39264"><div><strong>Mucopolysaccharidosis, MPS-III-A</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>39264</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.">C0086647</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Mucopolysaccharidosis type III (MPS III) is a multisystem lysosomal storage disease characterized by progressive central nervous system degeneration manifest as severe intellectual disability (ID), developmental regression, and other neurologic manifestations including autism spectrum disorder (ASD), behavioral problems, and sleep disturbances. Disease onset is typically before age ten years. Disease course may be rapidly or slowly progressive; some individuals with an extremely attenuated disease course present in mid-to-late adulthood with early-onset dementia with or without a history of ID. Systemic manifestations can include musculoskeletal problems (joint stiffness, contractures, scoliosis, and hip dysplasia), hearing loss, respiratory tract and sinopulmonary infections, and cardiac disease (valvular thickening, defects in the cardiac conduction system). Neurologic decline is seen in all affected individuals; however, clinical severity varies within and among the four MPS III subtypes (defined by the enzyme involved) and even among members of the same family. Death usually occurs in the second or third decade of life secondary to neurologic regression or respiratory tract infections.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/39264">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_88601"><div><strong>Mucopolysaccharidosis, MPS-III-B</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>88601</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.">C0086648</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Mucopolysaccharidosis type III (MPS III) is a multisystem lysosomal storage disease characterized by progressive central nervous system degeneration manifest as severe intellectual disability (ID), developmental regression, and other neurologic manifestations including autism spectrum disorder (ASD), behavioral problems, and sleep disturbances. Disease onset is typically before age ten years. Disease course may be rapidly or slowly progressive; some individuals with an extremely attenuated disease course present in mid-to-late adulthood with early-onset dementia with or without a history of ID. Systemic manifestations can include musculoskeletal problems (joint stiffness, contractures, scoliosis, and hip dysplasia), hearing loss, respiratory tract and sinopulmonary infections, and cardiac disease (valvular thickening, defects in the cardiac conduction system). Neurologic decline is seen in all affected individuals; however, clinical severity varies within and among the four MPS III subtypes (defined by the enzyme involved) and even among members of the same family. Death usually occurs in the second or third decade of life secondary to neurologic regression or respiratory tract infections.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/88601">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_39477"><div><strong>Mucopolysaccharidosis, MPS-III-C</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>39477</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.">C0086649</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Mucopolysaccharidosis type III (MPS III) is a multisystem lysosomal storage disease characterized by progressive central nervous system degeneration manifest as severe intellectual disability (ID), developmental regression, and other neurologic manifestations including autism spectrum disorder (ASD), behavioral problems, and sleep disturbances. Disease onset is typically before age ten years. Disease course may be rapidly or slowly progressive; some individuals with an extremely attenuated disease course present in mid-to-late adulthood with early-onset dementia with or without a history of ID. Systemic manifestations can include musculoskeletal problems (joint stiffness, contractures, scoliosis, and hip dysplasia), hearing loss, respiratory tract and sinopulmonary infections, and cardiac disease (valvular thickening, defects in the cardiac conduction system). Neurologic decline is seen in all affected individuals; however, clinical severity varies within and among the four MPS III subtypes (defined by the enzyme involved) and even among members of the same family. Death usually occurs in the second or third decade of life secondary to neurologic regression or respiratory tract infections.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/39477">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_88602"><div><strong>Mucopolysaccharidosis, MPS-III-D</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>88602</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.">C0086650</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Mucopolysaccharidosis type III (MPS III) is a multisystem lysosomal storage disease characterized by progressive central nervous system degeneration manifest as severe intellectual disability (ID), developmental regression, and other neurologic manifestations including autism spectrum disorder (ASD), behavioral problems, and sleep disturbances. Disease onset is typically before age ten years. Disease course may be rapidly or slowly progressive; some individuals with an extremely attenuated disease course present in mid-to-late adulthood with early-onset dementia with or without a history of ID. Systemic manifestations can include musculoskeletal problems (joint stiffness, contractures, scoliosis, and hip dysplasia), hearing loss, respiratory tract and sinopulmonary infections, and cardiac disease (valvular thickening, defects in the cardiac conduction system). Neurologic decline is seen in all affected individuals; however, clinical severity varies within and among the four MPS III subtypes (defined by the enzyme involved) and even among members of the same family. Death usually occurs in the second or third decade of life secondary to neurologic regression or respiratory tract infections.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/88602">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_331466"><div><strong>Hypertrophic cardiomyopathy 6</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>331466</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.">C1833236</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Mutations in the PRKAG2 gene (602743) give rise to a moderate, essentially heart-specific, nonlysosomal glycogenosis with clinical onset typically in late adolescence or in the third decade of life, ventricular pre-excitation predisposing to supraventricular arrhythmias, mild to severe cardiac hypertrophy, enhanced risk of sudden cardiac death in midlife, and autosomal dominant inheritance with full penetrance (summary by Burwinkel et al., 2005).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/331466">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_331754"><div><strong>Hypertrophic cardiomyopathy 10</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>331754</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.">C1834460</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/331754">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_395232"><div><strong>Cardiomyopathy associated with myopathy and sudden death</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>395232</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.">C1859328</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove nowrap">See: <a href="/medgen/395232">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_462554"><div><strong>Hypertrophic cardiomyopathy 16</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>462554</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.">C3151204</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYOZ2 gene.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/462554">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_501195"><div><strong>Hypertrophic cardiomyopathy 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>501195</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.">C3495498</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Hypertrophic cardiomyopathy (HCM) is typically defined by the presence of unexplained left ventricular hypertrophy (LVH). Such LVH occurs in a non-dilated ventricle in the absence of other cardiac or systemic disease capable of producing the observed magnitude of increased LV wall thickness, such as pressure overload (e.g., long-standing hypertension, aortic stenosis) or storage/infiltrative disorders (e.g., Fabry disease, amyloidosis). The clinical manifestations of HCM range from asymptomatic LVH to progressive heart failure to sudden cardiac death (SCD), and vary from individual to individual even within the same family. Common symptoms include shortness of breath (particularly with exertion), chest pain, palpitations, orthostasis, presyncope, and syncope. Most often the LVH of HCM becomes apparent during adolescence or young adulthood, although it may also develop late in life, in infancy, or in childhood.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/501195">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1779612"><div><strong>Cardiomyopathy, familial hypertrophic, 28</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1779612</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.">C5543616</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Familial hypertrophic cardiomyopathy-28 (CMH28) is characterized by asymmetric septal hypertrophy, atrial fibrillation and nonsustained ventricular tachycardia, and risk of sudden death. Dyspnea is the most common symptom, but more than half of affected individuals are asymptomatic. Hypertrabeculation of the left ventricle with noncompaction has been observed in some patients (Ochoa et al., 2018).&#13; For a general phenotypic description and discussion of genetic heterogeneity of familial hypertrophic cardiomyopathy, see CMH1 (192600).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1779612">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1824081"><div><strong>Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1824081</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.">C5774308</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Hypertrophic cardiomyopathy-29 (CMH29) is characterized by recurrent syncope, dyspnea on exertion, and palpitations. The clinical phenotype is associated with a poor prognosis due to lethal arrhythmias and cardiac failure. Cardiac muscle biopsies show intermyofibrillar accumulation of glycogen and polyglucosan bodies within cardiomyocytes, and skeletal muscle accumulation of glycogen has also been observed (Hedberg-Oldfors et al., 2019).&#13; For a general phenotypic description and discussion of genetic heterogeneity of hypertrophic cardiomyopathy, see CMH1 (192600).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1824081">Condition Record</a></div></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_395232" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cardiomyopathy associated with myopathy and sudden death</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1779612" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cardiomyopathy, familial hypertrophic, 28</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1824081" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_501195" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypertrophic cardiomyopathy 1</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_331754" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypertrophic cardiomyopathy 10</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (11)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_462554" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypertrophic cardiomyopathy 16</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_331466" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypertrophic cardiomyopathy 6</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_39264" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis, MPS-III-A</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_88601" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis, MPS-III-B</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_39477" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis, MPS-III-C</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_88602" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis, MPS-III-D</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/35643740">A retrospective investigation to establish new screening approach for the detection of patients at high risk of Fabry disease in male left ventricular hypertrophy patients.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kubo T,
Amano M,
Takashio S,
Okumura T,
Yamamoto S,
Nabeta T,
Oikawa M,
Kurisu S,
Ochi Y,
Sugiura K,
Baba Y,
Kuroiwa H,
Hirota T,
Yamasaki N,
Ishii S,
Nochioka K,
Takeishi Y,
Yasuda S,
Tsujita K,
Izumi C,
Kitaoka H</span><br />
<span class="medgenPMjournal">J Cardiol</span>
2022 Oct;80(4):325-331.
Epub 2022 May 25
doi: 10.1016/j.jjcc.2022.05.003.
<span class="bold">PMID: </span><a href="/pubmed/35643740" target="_blank">35643740</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31699383">Aortic Stenosis With Severe Asymmetric Septal Hypertrophy: A Novel Management Strategy to Improve TAVR Outcomes.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Khan AA,
Tang GHL,
Engstrom K,
Khan M,
Patel N,
Dangas GD,
Sharma SK,
Kini A</span><br />
<span class="medgenPMjournal">JACC Cardiovasc Interv</span>
2019 Nov 11;12(21):2228-2230.
doi: 10.1016/j.jcin.2019.06.025.
<span class="bold">PMID: </span><a href="/pubmed/31699383" target="_blank">31699383</a></div>
<div class="nl"><a target="_blank" href="/pubmed/21163429">Obstetrical care in gestational diabetes and management of preterm labour.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Thiebaugeorges O,
Guyard-Boileau B</span><br />
<span class="medgenPMjournal">Diabetes Metab</span>
2010 Dec;36(6 Pt 2):672-81.
doi: 10.1016/j.diabet.2010.11.017.
<span class="bold">PMID: </span><a href="/pubmed/21163429" target="_blank">21163429</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22asymmetric%20septal%20hypertrophy%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 (6)</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/36278454">New Era: Mavacamten for Obstructive Hypertrophic Cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Woodland M,
Al-Horani RA</span><br />
<span class="medgenPMjournal">Cardiovasc Hematol Agents Med Chem</span>
2023;21(2):78-83.
doi: 10.2174/1871525721666221019095218.
<span class="bold">PMID: </span><a href="/pubmed/36278454" target="_blank">36278454</a><a href="/pmc/articles/PMC10249146" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34726536">Patterns of Replacement Fibrosis in Hypertrophic Cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Liu J,
Zhao S,
Yu S,
Wu G,
Wang D,
Liu L,
Song J,
Zhu Y,
Kang L,
Wang J,
Song L</span><br />
<span class="medgenPMjournal">Radiology</span>
2022 Feb;302(2):298-306.
Epub 2021 Nov 2
doi: 10.1148/radiol.2021210914.
<span class="bold">PMID: </span><a href="/pubmed/34726536" target="_blank">34726536</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25351510">Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lopes LR,
Syrris P,
Guttmann OP,
O'Mahony C,
Tang HC,
Dalageorgou C,
Jenkins S,
Hubank M,
Monserrat L,
McKenna WJ,
Plagnol V,
Elliott PM</span><br />
<span class="medgenPMjournal">Heart</span>
2015 Feb;101(4):294-301.
Epub 2014 Oct 28
doi: 10.1136/heartjnl-2014-306387.
<span class="bold">PMID: </span><a href="/pubmed/25351510" target="_blank">25351510</a><a href="/pmc/articles/PMC4345808" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/3487889">Asymmetric septal hypertrophy (ASH) in valvular aortic stenosis should not be resected at the time of surgery.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schulte HD,
Bircks W,
Horstkotte D,
Kerstholt J,
Preusse CJ,
Winter J</span><br />
<span class="medgenPMjournal">Z Kardiol</span>
1986;75 Suppl 2:201-6.
<span class="bold">PMID: </span><a href="/pubmed/3487889" target="_blank">3487889</a></div>
<div class="nl"><a target="_blank" href="/pubmed/6890100">Hypertrophic cardiomyopathy is a component of subacute necrotizing encephalomyelopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Rutledge JC,
Haas JE,
Monnat R,
Milstein JM</span><br />
<span class="medgenPMjournal">J Pediatr</span>
1982 Nov;101(5):706-10.
doi: 10.1016/s0022-3476(82)80295-3.
<span class="bold">PMID: </span><a href="/pubmed/6890100" target="_blank">6890100</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Asymmetric%20septal%20hypertrophy%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 (119)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/39389613">Comatose patient with asymmetric septal hypertrophy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Mannion J,
Wilkinson M</span><br />
<span class="medgenPMjournal">Heart</span>
2024 Oct 10;110(21):1261-1286.
doi: 10.1136/heartjnl-2024-324820.
<span class="bold">PMID: </span><a href="/pubmed/39389613" target="_blank">39389613</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25351510">Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lopes LR,
Syrris P,
Guttmann OP,
O'Mahony C,
Tang HC,
Dalageorgou C,
Jenkins S,
Hubank M,
Monserrat L,
McKenna WJ,
Plagnol V,
Elliott PM</span><br />
<span class="medgenPMjournal">Heart</span>
2015 Feb;101(4):294-301.
Epub 2014 Oct 28
doi: 10.1136/heartjnl-2014-306387.
<span class="bold">PMID: </span><a href="/pubmed/25351510" target="_blank">25351510</a><a href="/pmc/articles/PMC4345808" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/3042405">Valvular aortic stenosis and asymmetric septal hypertrophy: diagnostic considerations and clinical and therapeutic implications.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Panza JA,
Maron BJ</span><br />
<span class="medgenPMjournal">Eur Heart J</span>
1988 Apr;9 Suppl E:71-6.
doi: 10.1093/eurheartj/9.suppl_e.71.
<span class="bold">PMID: </span><a href="/pubmed/3042405" target="_blank">3042405</a></div>
<div class="nl"><a target="_blank" href="/pubmed/4608574">Asymmetric septal hypertrophy.</a></div>
<div class="portlet_content ln"><span class="medgenPMjournal">Ann Intern Med</span>
1974 Nov;81(5):650-80.
doi: 10.7326/0003-4819-81-5-650.
<span class="bold">PMID: </span><a href="/pubmed/4608574" target="_blank">4608574</a></div>
<div class="nl"><a target="_blank" href="/pubmed/4266759">Asymmetric septal hypertrophy (ASH): the unifying link in the IHSS disease spectrum. Observations regarding its pathogenesis, pathophysiology, and course.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Henry WL,
Clark CE,
Epstein SE</span><br />
<span class="medgenPMjournal">Circulation</span>
1973 Apr;47(4):827-32.
doi: 10.1161/01.cir.47.4.827.
<span class="bold">PMID: </span><a href="/pubmed/4266759" target="_blank">4266759</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Asymmetric%20septal%20hypertrophy%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 (196)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/37116014">Unique Case of Cardiomyopathy Secondary to Adrenal Adenoma (Primary-Aldosteronism).</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Mandal C,
Dutta PK</span><br />
<span class="medgenPMjournal">J Assoc Physicians India</span>
2023 Jan;71(1):1.
<span class="bold">PMID: </span><a href="/pubmed/37116014" target="_blank">37116014</a></div>
<div class="nl"><a target="_blank" href="/pubmed/36278454">New Era: Mavacamten for Obstructive Hypertrophic Cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Woodland M,
Al-Horani RA</span><br />
<span class="medgenPMjournal">Cardiovasc Hematol Agents Med Chem</span>
2023;21(2):78-83.
doi: 10.2174/1871525721666221019095218.
<span class="bold">PMID: </span><a href="/pubmed/36278454" target="_blank">36278454</a><a href="/pmc/articles/PMC10249146" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/16816450">Asymmetric septal hypertrophy complicated by dynamic left ventricular obstruction after intra-aortic balloon counterpulsation placement in the setting of anterior myocardial infarction.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cohen R,
Rivagorda J,
Elhadad S</span><br />
<span class="medgenPMjournal">J Invasive Cardiol</span>
2006 Jul;18(7):E207-8.
<span class="bold">PMID: </span><a href="/pubmed/16816450" target="_blank">16816450</a></div>
<div class="nl"><a target="_blank" href="/pubmed/6502935">Echocardiography in sarcoidosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gregor P,
Widimsky P,
Sladkova T,
Petrikova J,
Cervenka V,
Visek V</span><br />
<span class="medgenPMjournal">Jpn Heart J</span>
1984 Jul;25(4):499-508.
doi: 10.1536/ihj.25.499.
<span class="bold">PMID: </span><a href="/pubmed/6502935" target="_blank">6502935</a></div>
<div class="nl"><a target="_blank" href="/pubmed/6143406">Pheochromocytoma with asymmetric septal hypertrophy: conflicting therapies confronting anesthesiologists.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Elsten JL,
Jelenich SE,
Macnamara TE</span><br />
<span class="medgenPMjournal">South Med J</span>
1984 Apr;77(4):525-6.
doi: 10.1097/00007611-198404000-00032.
<span class="bold">PMID: </span><a href="/pubmed/6143406" target="_blank">6143406</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Asymmetric%20septal%20hypertrophy%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 (56)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/34726536">Patterns of Replacement Fibrosis in Hypertrophic Cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Liu J,
Zhao S,
Yu S,
Wu G,
Wang D,
Liu L,
Song J,
Zhu Y,
Kang L,
Wang J,
Song L</span><br />
<span class="medgenPMjournal">Radiology</span>
2022 Feb;302(2):298-306.
Epub 2021 Nov 2
doi: 10.1148/radiol.2021210914.
<span class="bold">PMID: </span><a href="/pubmed/34726536" target="_blank">34726536</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25351510">Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lopes LR,
Syrris P,
Guttmann OP,
O'Mahony C,
Tang HC,
Dalageorgou C,
Jenkins S,
Hubank M,
Monserrat L,
McKenna WJ,
Plagnol V,
Elliott PM</span><br />
<span class="medgenPMjournal">Heart</span>
2015 Feb;101(4):294-301.
Epub 2014 Oct 28
doi: 10.1136/heartjnl-2014-306387.
<span class="bold">PMID: </span><a href="/pubmed/25351510" target="_blank">25351510</a><a href="/pmc/articles/PMC4345808" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/3487889">Asymmetric septal hypertrophy (ASH) in valvular aortic stenosis should not be resected at the time of surgery.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schulte HD,
Bircks W,
Horstkotte D,
Kerstholt J,
Preusse CJ,
Winter J</span><br />
<span class="medgenPMjournal">Z Kardiol</span>
1986;75 Suppl 2:201-6.
<span class="bold">PMID: </span><a href="/pubmed/3487889" target="_blank">3487889</a></div>
<div class="nl"><a target="_blank" href="/pubmed/775283">Asymmetric septal hypertrophy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Don IJ</span><br />
<span class="medgenPMjournal">Minn Med</span>
1976 Apr;59(4):279-82.
<span class="bold">PMID: </span><a href="/pubmed/775283" target="_blank">775283</a></div>
<div class="nl"><a target="_blank" href="/pubmed/4266759">Asymmetric septal hypertrophy (ASH): the unifying link in the IHSS disease spectrum. Observations regarding its pathogenesis, pathophysiology, and course.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Henry WL,
Clark CE,
Epstein SE</span><br />
<span class="medgenPMjournal">Circulation</span>
1973 Apr;47(4):827-32.
doi: 10.1161/01.cir.47.4.827.
<span class="bold">PMID: </span><a href="/pubmed/4266759" target="_blank">4266759</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Asymmetric%20septal%20hypertrophy%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 (66)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/34726536">Patterns of Replacement Fibrosis in Hypertrophic Cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Liu J,
Zhao S,
Yu S,
Wu G,
Wang D,
Liu L,
Song J,
Zhu Y,
Kang L,
Wang J,
Song L</span><br />
<span class="medgenPMjournal">Radiology</span>
2022 Feb;302(2):298-306.
Epub 2021 Nov 2
doi: 10.1148/radiol.2021210914.
<span class="bold">PMID: </span><a href="/pubmed/34726536" target="_blank">34726536</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25351510">Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lopes LR,
Syrris P,
Guttmann OP,
O'Mahony C,
Tang HC,
Dalageorgou C,
Jenkins S,
Hubank M,
Monserrat L,
McKenna WJ,
Plagnol V,
Elliott PM</span><br />
<span class="medgenPMjournal">Heart</span>
2015 Feb;101(4):294-301.
Epub 2014 Oct 28
doi: 10.1136/heartjnl-2014-306387.
<span class="bold">PMID: </span><a href="/pubmed/25351510" target="_blank">25351510</a><a href="/pmc/articles/PMC4345808" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/6890100">Hypertrophic cardiomyopathy is a component of subacute necrotizing encephalomyelopathy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Rutledge JC,
Haas JE,
Monnat R,
Milstein JM</span><br />
<span class="medgenPMjournal">J Pediatr</span>
1982 Nov;101(5):706-10.
doi: 10.1016/s0022-3476(82)80295-3.
<span class="bold">PMID: </span><a href="/pubmed/6890100" target="_blank">6890100</a></div>
<div class="nl"><a target="_blank" href="/pubmed/6985764">Hypertrophic cardiomyopathy. Recent observations regarding the specificity of three hallmarks of the disease: asymmetric septal hypertrophy, septal disorganization and systolic anterior motion of the anterior mitral leaflet.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Maron BJ,
Epstein SE</span><br />
<span class="medgenPMjournal">Am J Cardiol</span>
1980 Jan;45(1):141-54.
doi: 10.1016/0002-9149(80)90232-5.
<span class="bold">PMID: </span><a href="/pubmed/6985764" target="_blank">6985764</a></div>
<div class="nl"><a target="_blank" href="/pubmed/4266759">Asymmetric septal hypertrophy (ASH): the unifying link in the IHSS disease spectrum. Observations regarding its pathogenesis, pathophysiology, and course.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Henry WL,
Clark CE,
Epstein SE</span><br />
<span class="medgenPMjournal">Circulation</span>
1973 Apr;47(4):827-32.
doi: 10.1161/01.cir.47.4.827.
<span class="bold">PMID: </span><a href="/pubmed/4266759" target="_blank">4266759</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Asymmetric%20septal%20hypertrophy%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 (75)</a></div></div>
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<div class="nl"><a target="_blank" href="/pubmed/36028969">Hypertrophic Cardiomyopathy in Saudi Arabia: A Systematic Review of the Epidemiological, Clinical, and Imaging Features.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Rajab BS</span><br />
<span class="medgenPMjournal">Curr Cardiol Rev</span>
2023;19(2):e250822208003.
doi: 10.2174/1573403X18666220825153725.
<span class="bold">PMID: </span><a href="/pubmed/36028969" target="_blank">36028969</a><a href="/pmc/articles/PMC10201901" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/21163429">Obstetrical care in gestational diabetes and management of preterm labour.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Thiebaugeorges O,
Guyard-Boileau B</span><br />
<span class="medgenPMjournal">Diabetes Metab</span>
2010 Dec;36(6 Pt 2):672-81.
doi: 10.1016/j.diabet.2010.11.017.
<span class="bold">PMID: </span><a href="/pubmed/21163429" target="_blank">21163429</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Asymmetric%20septal%20hypertrophy%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 (2)</a></div></div>
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