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<!--
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UID=870150
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ConceptID=C4024582
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormality of the musculature of the limbs</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>870150</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.">C4024582</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Abnormal limb muscles; Muscle issues in the arms and/or legs</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:0009127">HP:0009127</a></td></tr>
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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="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 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">Abnormality of the musculature of the limbs</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="matched_ds">Abnormality of the musculature of the limbs</span><ul><li><span class="TLline"><a href="/medgen/871296" ref="tree=MeSH" title="MedGen record for Abnormality of the musculature of the lower limbs">Abnormality of the musculature of the lower limbs</a></span><ul><li><span class="TLline"><a href="/medgen/867409" ref="tree=MeSH" title="MedGen record for Abnormal calf musculature morphology">Abnormal calf musculature morphology</a></span><ul><li><span class="TLline"><a href="/medgen/374276" ref="tree=MeSH" title="MedGen record for Calf muscle pseudohypertrophy">Calf muscle pseudohypertrophy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/871297" ref="tree=MeSH" title="MedGen record for Abnormality of the foot musculature">Abnormality of the foot musculature</a></span><ul><li><span class="TLline"><a href="/medgen/870171" ref="tree=MeSH" title="MedGen record for Amyotrophy of ankle musculature">Amyotrophy of ankle musculature</a></span></li><li><span class="TLline"><a href="/medgen/870289" ref="tree=MeSH" title="MedGen record for Flexion limitation of toes">Flexion limitation of toes</a></span></li><li><span class="TLline"><a href="/medgen/868722" ref="tree=MeSH" title="MedGen record for Toe extensor amyotrophy">Toe extensor amyotrophy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/871295" ref="tree=MeSH" title="MedGen record for Abnormality thigh musculature morphology">Abnormality thigh musculature morphology</a></span></li><li><span class="TLline"><a href="/medgen/605222" ref="tree=MeSH" title="MedGen record for Asymmetrical gluteal crease">Asymmetrical gluteal crease</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/871291" ref="tree=MeSH" title="MedGen record for Abnormality of the musculature of the upper limbs">Abnormality of the musculature of the upper limbs</a></span><ul><li><span class="TLline"><a href="/medgen/871298" ref="tree=MeSH" title="MedGen record for Abnormality of the musculature of the hand">Abnormality of the musculature of the hand</a></span><ul><li><span class="TLline"><a href="/medgen/869380" ref="tree=MeSH" title="MedGen record for Abnormality of the hypothenar eminence">Abnormality of the hypothenar eminence</a></span></li><li><span class="TLline"><a href="/medgen/867412" ref="tree=MeSH" title="MedGen record for Abnormality of the thenar eminence">Abnormality of the thenar eminence</a></span></li><li><span class="TLline"><a href="/medgen/66798" ref="tree=MeSH" title="MedGen record for Hand muscle weakness">Hand muscle weakness</a></span></li><li><span class="TLline"><a href="/medgen/334705" ref="tree=MeSH" title="MedGen record for Hypotrophy of the small hand muscles">Hypotrophy of the small hand muscles</a></span></li><li><span class="TLline"><a href="/medgen/322432" ref="tree=MeSH" title="MedGen record for Weakness of the intrinsic hand muscles">Weakness of the intrinsic hand muscles</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/867408" ref="tree=MeSH" title="MedGen record for Abnormality of the shoulder girdle musculature">Abnormality of the shoulder girdle musculature</a></span><ul><li><span class="TLline"><a href="/medgen/871283" ref="tree=MeSH" title="MedGen record for Amyotrophy involving the shoulder musculature">Amyotrophy involving the shoulder musculature</a></span></li><li><span class="TLline"><a href="/medgen/870769" ref="tree=MeSH" title="MedGen record for Pectoral muscle hypoplasia/aplasia">Pectoral muscle hypoplasia/aplasia</a></span></li><li><span class="TLline"><a href="/medgen/66822" ref="tree=MeSH" title="MedGen record for Scapular winging">Scapular winging</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1864131" ref="tree=MeSH" title="MedGen record for Poly-hill sign">Poly-hill sign</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/870149" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia involving the musculature of the extremities">Aplasia/Hypoplasia involving the musculature of the extremities</a></span><ul><li><span class="TLline"><a href="/medgen/871282" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia involving the musculature of the upper limbs">Aplasia/Hypoplasia involving the musculature of the upper limbs</a></span><ul><li><span class="TLline"><a href="/medgen/871281" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia involving the musculature of the upper arm">Aplasia/Hypoplasia involving the musculature of the upper arm</a></span></li><li><span class="TLline"><a href="/medgen/871284" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia involving the shoulder musculature">Aplasia/Hypoplasia involving the shoulder musculature</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/869778" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia of the musculature of the thigh">Aplasia/Hypoplasia of the musculature of the thigh</a></span><ul><li><span class="TLline"><a href="/medgen/869777" ref="tree=MeSH" title="MedGen record for Aplasia/Hypoplasia of the quadriceps">Aplasia/Hypoplasia of the quadriceps</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/870484" ref="tree=MeSH" title="MedGen record for Asymmetric limb muscle stiffness">Asymmetric limb muscle stiffness</a></span></li><li><span class="TLline"><a href="/medgen/870172" ref="tree=MeSH" title="MedGen record for Generalized weakness of limb muscles">Generalized weakness of limb muscles</a></span></li><li><span class="TLline"><a href="/medgen/333083" ref="tree=MeSH" title="MedGen record for Limb hypertonia">Limb hypertonia</a></span><ul><li><span class="TLline"><a href="/medgen/375612" ref="tree=MeSH" title="MedGen record for Lower limb hypertonia">Lower limb hypertonia</a></span></li><li><span class="TLline"><a href="/medgen/867515" ref="tree=MeSH" title="MedGen record for Upper limb hypertonia">Upper limb hypertonia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/107956" ref="tree=MeSH" title="MedGen record for Limb muscle weakness">Limb muscle weakness</a></span><ul><li><span class="TLline"><a href="/medgen/356163" ref="tree=MeSH" title="MedGen record for Foot dorsiflexor weakness">Foot dorsiflexor weakness</a></span></li><li><span class="TLline"><a href="/medgen/324478" ref="tree=MeSH" title="MedGen record for Lower limb muscle weakness">Lower limb muscle weakness</a></span><ul><li><span class="TLline"><a href="/medgen/324514" ref="tree=MeSH" title="MedGen record for Distal lower limb muscle weakness">Distal lower limb muscle weakness</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/305607" ref="tree=MeSH" title="MedGen record for Upper limb muscle weakness">Upper limb muscle weakness</a></span><ul><li><span class="TLline"><a href="/medgen/533950" ref="tree=MeSH" title="MedGen record for Wrist drop">Wrist drop</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/330868" ref="tree=MeSH" title="MedGen record for Limb-girdle muscle atrophy">Limb-girdle muscle atrophy</a></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></li><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/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/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/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/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></li><li><span class="TLline"><a href="/medgen/424705" ref="tree=MeSH" title="MedGen record for Sarcoglycanopathy">Sarcoglycanopathy</a></span></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><li><span class="TLline"><a href="/medgen/347625" ref="tree=MeSH" title="MedGen record for Limb-girdle muscle weakness">Limb-girdle muscle weakness</a></span><ul><li><span class="TLline"><a href="/medgen/96534" ref="tree=MeSH" title="MedGen record for Pelvic girdle muscle weakness">Pelvic girdle muscle weakness</a></span><ul><li><span class="TLline"><a href="/medgen/1782499" ref="tree=MeSH" title="MedGen record for Hip adductor weakness">Hip adductor weakness</a></span></li><li><span class="TLline"><a href="/medgen/481355" ref="tree=MeSH" title="MedGen record for Hip flexor weakness">Hip flexor weakness</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/96533" ref="tree=MeSH" title="MedGen record for Shoulder girdle muscle weakness">Shoulder girdle muscle weakness</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/348365" ref="tree=MeSH" title="MedGen record for Proximal limb muscle stiffness">Proximal limb muscle stiffness</a></span></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</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>
|
||
<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/21411476">Predictive value of molar bite force on Class II functional appliance treatment outcomes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Antonarakis GS,
|
||
Kjellberg H,
|
||
Kiliaridis S</span><br />
|
||
<span class="medgenPMjournal">Eur J Orthod</span>
|
||
2012 Apr;34(2):244-9.
|
||
Epub 2011 Mar 16
|
||
doi: 10.1093/ejo/cjq184.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21411476" target="_blank">21411476</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16022217">Chronic exertional compartment syndrome: diagnosis and management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bong MR,
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||
Polatsch DB,
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||
Jazrawi LM,
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||
Rokito AS</span><br />
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||
<span class="medgenPMjournal">Bull Hosp Jt Dis</span>
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||
2005;62(3-4):77-84.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16022217" target="_blank">16022217</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9661242">Orthopedic management of neuromuscular disorders in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Birch JG</span><br />
|
||
<span class="medgenPMjournal">Semin Pediatr Neurol</span>
|
||
1998 Jun;5(2):78-91.
|
||
doi: 10.1016/s1071-9091(98)80024-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9661242" target="_blank">9661242</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormality%20of%20the%20musculature%20of%20the%20limbs)%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 (3)</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">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37591693">Reclassification of the HPGD p.Ala13Glu variant causing primary hypertrophic osteoarthropathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alban JJ,
|
||
Arango-Ramirez A,
|
||
Olave-Rodriguez JA,
|
||
Nastasi-Catanese JA,
|
||
Rodriguez LX</span><br />
|
||
<span class="medgenPMjournal">Cold Spring Harb Mol Case Stud</span>
|
||
2023 Dec;9(4)
|
||
Epub 2024 Jan 10
|
||
doi: 10.1101/mcs.a006291.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37591693" target="_blank">37591693</a><a href="/pmc/articles/PMC10815292" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31127036">MYL2-associated congenital fiber-type disproportion and cardiomyopathy with variants in additional neuromuscular disease genes; the dilemma of panel testing.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marttila M,
|
||
Win W,
|
||
Al-Ghamdi F,
|
||
Abdel-Hamid HZ,
|
||
Lacomis D,
|
||
Beggs AH</span><br />
|
||
<span class="medgenPMjournal">Cold Spring Harb Mol Case Stud</span>
|
||
2019 Aug;5(4)
|
||
Epub 2019 Aug 1
|
||
doi: 10.1101/mcs.a004184.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31127036" target="_blank">31127036</a><a href="/pmc/articles/PMC6672024" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20musculature%20of%20the%20limbs%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 (2)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37591693">Reclassification of the HPGD p.Ala13Glu variant causing primary hypertrophic osteoarthropathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alban JJ,
|
||
Arango-Ramirez A,
|
||
Olave-Rodriguez JA,
|
||
Nastasi-Catanese JA,
|
||
Rodriguez LX</span><br />
|
||
<span class="medgenPMjournal">Cold Spring Harb Mol Case Stud</span>
|
||
2023 Dec;9(4)
|
||
Epub 2024 Jan 10
|
||
doi: 10.1101/mcs.a006291.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37591693" target="_blank">37591693</a><a href="/pmc/articles/PMC10815292" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36997313">Progressive metastatic infantile fibrosarcoma with multiple acquired mutations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Furtado LV,
|
||
Kacar M,
|
||
Mostafavi R,
|
||
Shi Z,
|
||
Ruiz R,
|
||
Koo SC,
|
||
Santiago T,
|
||
Segers B,
|
||
Krasin MJ,
|
||
Abramson ZR,
|
||
Shulkin B,
|
||
Talbot LJ,
|
||
Pappo A,
|
||
Gartrell J</span><br />
|
||
<span class="medgenPMjournal">Cold Spring Harb Mol Case Stud</span>
|
||
2023 Apr;9(2)
|
||
Epub 2023 May 9
|
||
doi: 10.1101/mcs.a006277.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36997313" target="_blank">36997313</a><a href="/pmc/articles/PMC10240842" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20musculature%20of%20the%20limbs%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 (2)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37591693">Reclassification of the HPGD p.Ala13Glu variant causing primary hypertrophic osteoarthropathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alban JJ,
|
||
Arango-Ramirez A,
|
||
Olave-Rodriguez JA,
|
||
Nastasi-Catanese JA,
|
||
Rodriguez LX</span><br />
|
||
<span class="medgenPMjournal">Cold Spring Harb Mol Case Stud</span>
|
||
2023 Dec;9(4)
|
||
Epub 2024 Jan 10
|
||
doi: 10.1101/mcs.a006291.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37591693" target="_blank">37591693</a><a href="/pmc/articles/PMC10815292" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormality%20of%20the%20musculature%20of%20the%20limbs%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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||
|
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|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
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<div class="portlet mgSection" id="ID_113">
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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=Abnormality%20of%20the%20musculature%20of%20the%20limbs" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet mgSection" id="ID_121">
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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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