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<!--
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UID=330868
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ConceptID=C1842552
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Limb-girdle muscle atrophy</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>330868</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) Click for more information.">C1842552</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>Limb-girdle myopathy; Wasting of limb-girdle muscle</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:0003797">HP:0003797</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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<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>
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||
<div class="portlet_content ln">Muscular atrophy affecting the muscles of the limb girdle. [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>
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<div class="portlet mgSection" id="ID_118">
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<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>
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<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="TLline">Limb-girdle muscle atrophy</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/536898" ref="tree=MeSH" title="MedGen record for Abnormality of limbs">Abnormality of limbs</a></span><ul><li><span class="TLline"><a href="/medgen/870150" ref="tree=MeSH" title="MedGen record for Abnormality of the musculature of the limbs">Abnormality of the musculature of the limbs</a></span><ul><li><span class="matched_ds">Limb-girdle muscle atrophy</span><ul><li><span class="TLline"><a href="/medgen/151940" ref="tree=MeSH" title="MedGen record for Limb-girdle muscular dystrophy">Limb-girdle muscular dystrophy</a></span><ul><li><span class="TLline"><a href="/medgen/419194" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy">Autosomal recessive limb-girdle muscular dystrophy</a></span><ul><li><span class="TLline"><a href="/medgen/358391" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2A">Autosomal recessive limb-girdle muscular dystrophy type 2A</a></span></li><li><span class="TLline"><a href="/medgen/338149" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2B">Autosomal recessive limb-girdle muscular dystrophy type 2B</a></span></li><li><span class="TLline"><a href="/medgen/98045" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2C">Autosomal recessive limb-girdle muscular dystrophy type 2C</a></span></li><li><span class="TLline"><a href="/medgen/424706" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2D">Autosomal recessive limb-girdle muscular dystrophy type 2D</a></span></li><li><span class="TLline"><a href="/medgen/347674" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2E">Autosomal recessive limb-girdle muscular dystrophy type 2E</a></span></li><li><span class="TLline"><a href="/medgen/331308" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2F">Autosomal recessive limb-girdle muscular dystrophy type 2F</a></span></li><li><span class="TLline"><a href="/medgen/400895" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2G">Autosomal recessive limb-girdle muscular dystrophy type 2G</a></span></li><li><span class="TLline"><a href="/medgen/339580" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2I">Autosomal recessive limb-girdle muscular dystrophy type 2I</a></span></li><li><span class="TLline"><a href="/medgen/324741" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2J">Autosomal recessive limb-girdle muscular dystrophy type 2J</a></span></li><li><span class="TLline"><a href="/medgen/332193" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2K">Autosomal recessive limb-girdle muscular dystrophy type 2K</a></span></li><li><span class="TLline"><a href="/medgen/370102" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2L">Autosomal recessive limb-girdle muscular dystrophy type 2L</a></span></li><li><span class="TLline"><a href="/medgen/370585" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2M">Autosomal recessive limb-girdle muscular dystrophy type 2M</a></span></li><li><span class="TLline"><a href="/medgen/461768" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2N">Autosomal recessive limb-girdle muscular dystrophy type 2N</a></span></li><li><span class="TLline"><a href="/medgen/461767" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2O">Autosomal recessive limb-girdle muscular dystrophy type 2O</a></span></li><li><span class="TLline"><a href="/medgen/1386785" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2P">Autosomal recessive limb-girdle muscular dystrophy type 2P</a></span></li><li><span class="TLline"><a href="/medgen/462339" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2Q">Autosomal recessive limb-girdle muscular dystrophy type 2Q</a></span></li><li><span class="TLline"><a href="/medgen/934627" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2R1">Autosomal recessive limb-girdle muscular dystrophy type 2R1</a></span></li><li><span class="TLline"><a href="/medgen/1377325" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2T">Autosomal recessive limb-girdle muscular dystrophy type 2T</a></span></li><li><span class="TLline"><a href="/medgen/1683417" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2U">Autosomal recessive limb-girdle muscular dystrophy type 2U</a></span></li><li><span class="TLline"><a href="/medgen/897675" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2W">Autosomal recessive limb-girdle muscular dystrophy type 2W</a></span></li><li><span class="TLline"><a href="/medgen/1799561" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2X">Autosomal recessive limb-girdle muscular dystrophy type 2X</a></span></li><li><span class="TLline"><a href="/medgen/1385152" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type 2Y">Autosomal recessive limb-girdle muscular dystrophy type 2Y</a></span></li><li><span class="TLline"><a href="/medgen/1385598" ref="tree=MeSH" title="MedGen record for Autosomal recessive limb-girdle muscular dystrophy type R18">Autosomal recessive limb-girdle muscular dystrophy type R18</a></span></li><li><span class="TLline"><a href="/medgen/863621" ref="tree=MeSH" title="MedGen record for Limb-girdle muscular dystrophy due to POMK deficiency">Limb-girdle muscular dystrophy due to POMK deficiency</a></span></li><li><span class="TLline"><a href="/medgen/105341" ref="tree=MeSH" title="MedGen record for Muscle eye brain disease">Muscle eye brain disease</a></span></li><li><span class="TLline"><a href="/medgen/1648462" ref="tree=MeSH" title="MedGen record for Muscular dystrophy, limb-girdle, autosomal recessive 23">Muscular dystrophy, limb-girdle, autosomal recessive 23</a></span></li><li><span class="TLline"><a href="/medgen/413465" ref="tree=MeSH" title="MedGen record for Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4">Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4</a></span></li><li><span class="TLline"><a href="/medgen/335764" ref="tree=MeSH" title="MedGen record for Muscular dystrophy-dystroglycanopathy type B5">Muscular dystrophy-dystroglycanopathy type B5</a></span></li><li><span class="TLline"><a href="/medgen/1830095" ref="tree=MeSH" title="MedGen record for POMGNT2-related limb-girdle muscular dystrophy R24">POMGNT2-related limb-girdle muscular dystrophy R24</a></span></li><li><span class="TLline"><a href="/medgen/419874" ref="tree=MeSH" title="MedGen record for Qualitative or quantitative defects of dysferlin">Qualitative or quantitative defects of dysferlin</a></span></li><li><span class="TLline"><a href="/medgen/424705" ref="tree=MeSH" title="MedGen record for Sarcoglycanopathy">Sarcoglycanopathy</a></span></li><li><span class="TLline"><a href="/medgen/78750" ref="tree=MeSH" title="MedGen record for Sarcotubular myopathy">Sarcotubular myopathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/371358" ref="tree=MeSH" title="MedGen record for Limb-Girdle Muscular Dystrophy Type 1C">Limb-Girdle Muscular Dystrophy Type 1C</a></span></li><li><span class="TLline"><a href="/medgen/1826162" ref="tree=MeSH" title="MedGen record for Muscular dystrophy, limb-girdle, autosomal dominant">Muscular dystrophy, limb-girdle, autosomal dominant</a></span><ul><li><span class="TLline"><a href="/medgen/1648441" ref="tree=MeSH" title="MedGen record for Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)">Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)</a></span></li><li><span class="TLline"><a href="/medgen/333983" ref="tree=MeSH" title="MedGen record for Autosomal dominant limb-girdle muscular dystrophy type 1F">Autosomal dominant limb-girdle muscular dystrophy type 1F</a></span></li><li><span class="TLline"><a href="/medgen/322993" ref="tree=MeSH" title="MedGen record for Autosomal dominant limb-girdle muscular dystrophy type 1G">Autosomal dominant limb-girdle muscular dystrophy type 1G</a></span></li><li><span class="TLline"><a href="/medgen/462136" ref="tree=MeSH" title="MedGen record for Autosomal dominant limb-girdle muscular dystrophy type 1H">Autosomal dominant limb-girdle muscular dystrophy type 1H</a></span></li><li><span class="TLline"><a href="/medgen/993836" ref="tree=MeSH" title="MedGen record for Calpain-3-related limb-girdle muscular dystrophy D4">Calpain-3-related limb-girdle muscular dystrophy D4</a></span></li><li><span class="TLline"><a href="/medgen/1826055" ref="tree=MeSH" title="MedGen record for Caveolinopathy">Caveolinopathy</a></span></li><li><span class="TLline"><a href="/medgen/330449" ref="tree=MeSH" title="MedGen record for Desmin-related myofibrillar myopathy">Desmin-related myofibrillar myopathy</a></span></li><li><span class="TLline"><a href="/medgen/98048" ref="tree=MeSH" title="MedGen record for Emery-Dreifuss muscular dystrophy 2, autosomal dominant">Emery-Dreifuss muscular dystrophy 2, autosomal dominant</a></span></li><li><span class="TLline"><a href="/medgen/811509" ref="tree=MeSH" title="MedGen record for Myofibrillar myopathy 3">Myofibrillar myopathy 3</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/867170" ref="tree=MeSH" title="MedGen record for Pelvic girdle amyotrophy">Pelvic girdle amyotrophy</a></span></li><li><span class="TLline"><a href="/medgen/339837" ref="tree=MeSH" title="MedGen record for Shoulder girdle muscle atrophy">Shoulder girdle muscle atrophy</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</div>
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<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>
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<div class="portlet_content ln clinfeat">
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<div class="divPopper rprt" id="rdis_424706"><div><strong>Autosomal recessive limb-girdle muscular dystrophy type 2D</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>424706</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) Click for more information.">C2936332</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Autosomal recessive limb-girdle muscular dystrophy-3 (LGMDR3) affects mainly the proximal muscles and results in difficulty walking. Most individuals have onset in childhood; the disorder is progressive. Other features may include scapular winging, calf pseudohypertrophy, and contractures. Cardiomyopathy has rarely been reported (summary by Babameto-Laku et al., 2011). For a discussion of genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy, see LGMDR1 (253600).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/424706">Condition Record</a></div></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_424706" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive limb-girdle muscular dystrophy type 2D</a></div></div>
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</div>
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<div class="portlet mgSection" id="ID_105">
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<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>
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<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>
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<div class="nl"><a target="_blank" href="/pubmed/38383972">Non-viral delivery of nucleic acid for treatment of rare diseases of the muscle.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Rao D,
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Ganguli M</span><br />
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<span class="medgenPMjournal">J Biosci</span>
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2024;49
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<span class="bold">PMID: </span><a href="/pubmed/38383972" target="_blank">38383972</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/37856057">MicroRNAs as a Tool for Differential Diagnosis of Neuromuscular Disorders.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mousa NO,
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Abdellatif A,
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||
Fahmy N,
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||
El-Fawal H,
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||
Osman A</span><br />
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<span class="medgenPMjournal">Neuromolecular Med</span>
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2023 Dec;25(4):603-615.
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||
Epub 2023 Oct 19
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||
doi: 10.1007/s12017-023-08763-0.
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||
<span class="bold">PMID: </span><a href="/pubmed/37856057" target="_blank">37856057</a><a href="/pmc/articles/PMC10721695" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27197572">Prenatal diagnosis of congenital myopathies and muscular dystrophies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Massalska D,
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||
Zimowski JG,
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||
Bijok J,
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||
Kucińska-Chahwan A,
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||
Łusakowska A,
|
||
Jakiel G,
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||
Roszkowski T</span><br />
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||
<span class="medgenPMjournal">Clin Genet</span>
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||
2016 Sep;90(3):199-210.
|
||
Epub 2016 Jun 2
|
||
doi: 10.1111/cge.12801.
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||
<span class="bold">PMID: </span><a href="/pubmed/27197572" target="_blank">27197572</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(limb-girdle%20muscle%20atrophy)%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 (8)</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/20482818">Depression in Myotonic Dystrophy type 1: clinical and neuronal correlates.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Winblad S,
|
||
Jensen C,
|
||
Månsson JE,
|
||
Samuelsson L,
|
||
Lindberg C</span><br />
|
||
<span class="medgenPMjournal">Behav Brain Funct</span>
|
||
2010 May 19;6:25.
|
||
doi: 10.1186/1744-9081-6-25.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20482818" target="_blank">20482818</a><a href="/pmc/articles/PMC2881877" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2324771">Limb girdle syndromes. Clinical, morphological and electrophysiological studies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Panegyres PK,
|
||
Mastaglia FL,
|
||
Kakulas BA</span><br />
|
||
<span class="medgenPMjournal">J Neurol Sci</span>
|
||
1990 Feb;95(2):201-18.
|
||
doi: 10.1016/0022-510x(90)90243-g.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2324771" target="_blank">2324771</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Limb-girdle%20muscle%20atrophy%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 (2)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/20482818">Depression in Myotonic Dystrophy type 1: clinical and neuronal correlates.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Winblad S,
|
||
Jensen C,
|
||
Månsson JE,
|
||
Samuelsson L,
|
||
Lindberg C</span><br />
|
||
<span class="medgenPMjournal">Behav Brain Funct</span>
|
||
2010 May 19;6:25.
|
||
doi: 10.1186/1744-9081-6-25.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20482818" target="_blank">20482818</a><a href="/pmc/articles/PMC2881877" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Limb-girdle%20muscle%20atrophy%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 (1)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
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||
|
||
</div>
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<div class=" bottom">
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</div>
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||
</div>
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||
<div class="supplemental col three_col last">
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div>
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||
|
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<!-- MedGen supplemental column starts here -->
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<div class="rightCol mgCol">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Limb-girdle%20muscle%20atrophy" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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</div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></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=(limb-girdle%20muscle%20atrophy)%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(%22Limb-girdle%20muscle%20atrophy%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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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Limb-girdle%20muscle%20atrophy" target="_blank">MedlinePlus</a></li></ul></div>
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