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<meta name="keywords" content="C1839832, cardiomyopathy, noncompaction, disease or syndrome, finding, noncompaction cardiomyopathy, noncompaction of the ventricular myocardium, noncompaction of ventricular myocardium, spongiform cardiomyopathy, 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="A type of cardiomyopathy characterized anatomically by deep trabeculations in the ventricular wall, which define recesses communicating with the main ventricular chamber." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Noncompaction cardiomyopathy (Concept Id: C1839832)
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<!--
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UID=326592
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ConceptID=C1839832
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Noncompaction cardiomyopathy</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>326592</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."><span class="highlight" style="background-color:">C1839832</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
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<td>Cardiomyopathy, noncompaction; Noncompaction of ventricular myocardium</td></tr>
|
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<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0012817">HP:0012817</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">A type of cardiomyopathy characterized anatomically by deep trabeculations in the ventricular wall, which define recesses communicating with the main ventricular chamber. [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">Noncompaction cardiomyopathy</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/2848" ref="tree=MeSH" title="MedGen record for Disorder of cardiovascular system">Disorder of cardiovascular system</a></span><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="matched_ds">Noncompaction cardiomyopathy</span><ul><li><span class="TLline"><a href="/medgen/868319" ref="tree=MeSH" title="MedGen record for Biventricular noncompaction cardiomyopathy">Biventricular noncompaction cardiomyopathy</a></span></li><li><span class="TLline"><a href="/medgen/866782" ref="tree=MeSH" title="MedGen record for Left ventricular noncompaction cardiomyopathy">Left ventricular noncompaction cardiomyopathy</a></span><ul><li><span class="TLline"><a href="/medgen/767410" ref="tree=MeSH" title="MedGen record for Left ventricular noncompaction 7">Left ventricular noncompaction 7</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/868320" ref="tree=MeSH" title="MedGen record for Right ventricular noncompaction cardiomyopathy">Right ventricular noncompaction cardiomyopathy</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
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||
|
||
<div class="portlet mgSection" id="ID_112">
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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">
|
||
<div class="divPopper rprt" id="rdis_334629"><div><strong>Chromosome 1p36 deletion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>334629</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.">C1842870</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The constitutional deletion of chromosome 1p36 results in a syndrome with multiple congenital anomalies and mental retardation (Shapira et al., 1997). Monosomy 1p36 is the most common terminal deletion syndrome in humans, occurring in 1 in 5,000 births (Shaffer and Lupski, 2000; Heilstedt et al., 2003). See also neurodevelopmental disorder with or without anomalies of the brain, eye, or heart (NEDBEH; 616975), which shows overlapping features and is caused by heterozygous mutation in the RERE gene (605226) on proximal chromosome 1p36. See also Radio-Tartaglia syndrome (RATARS; 619312), caused by mutation in the SPEN gene (613484) on chromosome 1p36, which shows overlapping features.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/334629">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_375801"><div><strong>Roifman syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>375801</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.">C1846059</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">RNU4atac-opathy encompasses the phenotypic spectrum of biallelic RNU4ATAC pathogenic variants, including the three historically designated clinical phenotypes microcephalic osteodysplastic primordial dwarfism type I/III (MOPDI), Roifman syndrome, and Lowry-Wood syndrome, as well as varying combinations of the disease features / system involvement that do not match specific defined phenotypes. Findings present in all affected individuals include growth restriction, microcephaly, skeletal dysplasia, and cognitive impairment. Less common but variable findings include brain anomalies, seizures, strokes, immunodeficiency, and cardiac anomalies, as well as ophthalmologic, skin, renal, gastrointestinal, hearing, and endocrine involvement.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/375801">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_347542"><div><strong>3-methylglutaconic aciduria type 5</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347542</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.">C1857776</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">3-Methylglutaconic aciduria type V (MGCA5) is an autosomal recessive disorder characterized by the onset of dilated or noncompaction cardiomyopathy in infancy or early childhood. Many patients die of cardiac failure. Other features include microcytic anemia, growth retardation, mild ataxia, mild muscle weakness, genital anomalies in males, and increased urinary excretion of 3-methylglutaconic acid. Some patients may have optic atrophy or delayed psychomotor development (summary by Davey et al., 2006 and Ojala et al., 2012). For a discussion of genetic heterogeneity of 3-methylglutaconic aciduria, see MGCA type I (250950).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/347542">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_349005"><div><strong>Left ventricular noncompaction 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>349005</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.">C1858725</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Left ventricular noncompaction (LVNC) is characterized by numerous prominent trabeculations and deep intertrabecular recesses in hypertrophied and hypokinetic segments of the left ventricle (Sasse-Klaassen et al., 2004). The mechanistic basis is thought to be an intrauterine arrest of myocardial development with lack of compaction of the loose myocardial meshwork. LVNC may occur in isolation or in association with congenital heart disease. Distinctive morphologic features can be recognized on 2-dimensional echocardiography (Kurosaki et al., 1999). Noncompaction of the ventricular myocardium is sometimes referred to as spongy myocardium. Stollberger et al. (2002) commented that the term 'isolated LVNC,' meaning LVNC without coexisting cardiac abnormalities, is misleading, because additional cardiac abnormalities are found in nearly all patients with LVNC. Genetic Heterogeneity of Left Ventricular Noncompaction A locus for autosomal dominant left ventricular noncompaction has been identified on chromosome 11p15 (LVNC2; 609470). LVNC3 (see 605906) is caused by mutation in the LDB3 gene (605906) on chromosome 10q23. LVNC4 (see 613424) is caused by mutation in the ACTC1 gene (102540) on chromosome 15q14. LVNC5 (see 613426) is caused by mutation in the MYH7 gene (160760) on chromosome 14q12. LVNC6 (see 601494) is caused by mutation in the TNNT2 gene (191045) on chromosome 1q32. LVNC7 (615092) is caused by mutation in the MIB1 gene (608677) on chromosome 18q11. LVNC8 (615373) is caused by mutation in the PRDM16 gene (605557) on chromosome 1p36. LVNC9 (see 611878) is caused by mutation in the TPM1 gene (191010) on chromosome 15q22. LVNC10 (615396) is caused by mutation in the MYBPC3 gene (600958) on chromosome 11p11. LVNC can also occur as part of an X-linked disorder, Barth syndrome (302060), caused by mutation in the TAZ gene (300394) on chromosome Xq28.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/349005">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_347542" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">3-methylglutaconic aciduria type 5</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_334629" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chromosome 1p36 deletion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_349005" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Left ventricular noncompaction 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_375801" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Roifman syndrome</a></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/31008770">Left Ventricular Noncompaction: Diagnostic Approach, Prognostic Evaluation, and Management Strategies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Di Fusco SA,
|
||
Lucà F,
|
||
Madeo A,
|
||
Massimiliano Rao C,
|
||
Iorio A,
|
||
Rizzo M,
|
||
Dalila Luisella Delcre S,
|
||
Colivicchi F,
|
||
Gabrielli D,
|
||
Paolo Pino G,
|
||
Massimo Gulizia M</span><br />
|
||
<span class="medgenPMjournal">Cardiol Rev</span>
|
||
2020 May/Jun;28(3):125-134.
|
||
doi: 10.1097/CRD.0000000000000251.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31008770" target="_blank">31008770</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31771441">Systematic Review of Genotype-Phenotype Correlations in Noncompaction Cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van Waning JI,
|
||
Moesker J,
|
||
Heijsman D,
|
||
Boersma E,
|
||
Majoor-Krakauer D</span><br />
|
||
<span class="medgenPMjournal">J Am Heart Assoc</span>
|
||
2019 Dec 3;8(23):e012993.
|
||
Epub 2019 Nov 27
|
||
doi: 10.1161/JAHA.119.012993.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31771441" target="_blank">31771441</a><a href="/pmc/articles/PMC6912966" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29903360">Genotype, Family History, and Outcomes in Noncompaction Cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bermudez-Jiménez FJ,
|
||
Jiménez-Jáimez J</span><br />
|
||
<span class="medgenPMjournal">J Am Coll Cardiol</span>
|
||
2018 Jun 19;71(24):2864.
|
||
doi: 10.1016/j.jacc.2018.03.527.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29903360" target="_blank">29903360</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22noncompaction%20cardiomyopathy%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 (10)</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/39477714">Special considerations for the stabilization and resuscitation of patients with cardiac disease in the Neonatal Intensive Care Unit.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Johnson BA,
|
||
Shepherd J,
|
||
Bhombal S,
|
||
Ali N,
|
||
Joynt C</span><br />
|
||
<span class="medgenPMjournal">Semin Perinatol</span>
|
||
2024 Dec;48(8):151989.
|
||
Epub 2024 Oct 8
|
||
doi: 10.1016/j.semperi.2024.151989.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39477714" target="_blank">39477714</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37016994">Considerations for specific cardiomyopathies during pregnancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Abrams M,
|
||
Magun E,
|
||
DeFilippis EM</span><br />
|
||
<span class="medgenPMjournal">Curr Opin Cardiol</span>
|
||
2023 May 1;38(3):233-240.
|
||
Epub 2023 Mar 1
|
||
doi: 10.1097/HCO.0000000000001033.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37016994" target="_blank">37016994</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30848673">Dilated cardiomyopathy in a pediatric population: etiology and outcome predictors - a single-center experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ciuca C,
|
||
Ragni L,
|
||
Hasan T,
|
||
Balducci A,
|
||
Angeli E,
|
||
Prandstraller D,
|
||
Egidy-Assenza G,
|
||
Donti A,
|
||
Bonvicini M,
|
||
Gargiulo GD</span><br />
|
||
<span class="medgenPMjournal">Future Cardiol</span>
|
||
2019 Mar;15(2):95-107.
|
||
Epub 2019 Mar 8
|
||
doi: 10.2217/fca-2018-0030.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30848673" target="_blank">30848673</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29447731">Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van Waning JI,
|
||
Caliskan K,
|
||
Hoedemaekers YM,
|
||
van Spaendonck-Zwarts KY,
|
||
Baas AF,
|
||
Boekholdt SM,
|
||
van Melle JP,
|
||
Teske AJ,
|
||
Asselbergs FW,
|
||
Backx APCM,
|
||
du Marchie Sarvaas GJ,
|
||
Dalinghaus M,
|
||
Breur JMPJ,
|
||
Linschoten MPM,
|
||
Verlooij LA,
|
||
Kardys I,
|
||
Dooijes D,
|
||
Lekanne Deprez RH,
|
||
IJpma AS,
|
||
van den Berg MP,
|
||
Hofstra RMW,
|
||
van Slegtenhorst MA,
|
||
Jongbloed JDH,
|
||
Majoor-Krakauer D</span><br />
|
||
<span class="medgenPMjournal">J Am Coll Cardiol</span>
|
||
2018 Feb 20;71(7):711-722.
|
||
doi: 10.1016/j.jacc.2017.12.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29447731" target="_blank">29447731</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21428140">Noncompaction cardiomyopathy--a review of eight cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Toste A,
|
||
Branco LM,
|
||
Galrinho A,
|
||
Lousinha A,
|
||
Fiarresga A,
|
||
Oliveira MM,
|
||
Abreu J,
|
||
Mendes JJ,
|
||
Ferreira L,
|
||
Leal A,
|
||
Ferreira RC</span><br />
|
||
<span class="medgenPMjournal">Rev Port Cardiol</span>
|
||
2010 Dec;29(12):1847-64.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21428140" target="_blank">21428140</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Noncompaction%20cardiomyopathy%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 (87)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32640777">Left ventricular noncompaction cardiomyopathy: diagnostic and therapeutic dilemmas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zienciuk-Krajka A,
|
||
Daniłowicz-Szymanowicz L,
|
||
Dorniak K,
|
||
Kaufmann D,
|
||
Raczak G</span><br />
|
||
<span class="medgenPMjournal">Kardiol Pol</span>
|
||
2020 Oct 23;78(10):1053-1054.
|
||
Epub 2020 Jul 8
|
||
doi: 10.33963/KP.15503.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32640777" target="_blank">32640777</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29447731">Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van Waning JI,
|
||
Caliskan K,
|
||
Hoedemaekers YM,
|
||
van Spaendonck-Zwarts KY,
|
||
Baas AF,
|
||
Boekholdt SM,
|
||
van Melle JP,
|
||
Teske AJ,
|
||
Asselbergs FW,
|
||
Backx APCM,
|
||
du Marchie Sarvaas GJ,
|
||
Dalinghaus M,
|
||
Breur JMPJ,
|
||
Linschoten MPM,
|
||
Verlooij LA,
|
||
Kardys I,
|
||
Dooijes D,
|
||
Lekanne Deprez RH,
|
||
IJpma AS,
|
||
van den Berg MP,
|
||
Hofstra RMW,
|
||
van Slegtenhorst MA,
|
||
Jongbloed JDH,
|
||
Majoor-Krakauer D</span><br />
|
||
<span class="medgenPMjournal">J Am Coll Cardiol</span>
|
||
2018 Feb 20;71(7):711-722.
|
||
doi: 10.1016/j.jacc.2017.12.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29447731" target="_blank">29447731</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29221698">Undulating Clinical Course of Noncompaction Cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dolader P,
|
||
Gran F,
|
||
Giralt G,
|
||
Ferrer Q,
|
||
Rosés-Noguer F,
|
||
Albert DC</span><br />
|
||
<span class="medgenPMjournal">Rev Esp Cardiol (Engl Ed)</span>
|
||
2018 Dec;71(12):1077-1079.
|
||
Epub 2017 Dec 6
|
||
doi: 10.1016/j.rec.2017.11.014.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29221698" target="_blank">29221698</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29267629">Limitations in the Diagnosis of Noncompaction Cardiomyopathy by Echocardiography.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hotta VT,
|
||
Tendolo SC,
|
||
Rodrigues ACT,
|
||
Fernandes F,
|
||
Nastari L,
|
||
Mady C</span><br />
|
||
<span class="medgenPMjournal">Arq Bras Cardiol</span>
|
||
2017 Nov;109(5):483-488.
|
||
doi: 10.5935/abc.20170152.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29267629" target="_blank">29267629</a><a href="/pmc/articles/PMC5729785" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27989498">Recent advancements in the molecular genetics of left ventricular noncompaction cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dong X,
|
||
Fan P,
|
||
Tian T,
|
||
Yang Y,
|
||
Xiao Y,
|
||
Yang K,
|
||
Liu Y,
|
||
Zhou X</span><br />
|
||
<span class="medgenPMjournal">Clin Chim Acta</span>
|
||
2017 Feb;465:40-44.
|
||
Epub 2016 Dec 15
|
||
doi: 10.1016/j.cca.2016.12.013.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27989498" target="_blank">27989498</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Noncompaction%20cardiomyopathy%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 (169)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37658577">Left ventricular noncompaction cardiomyopathy and short QT syndrome due to primary carnitine deficiency.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hanington OP,
|
||
Armstrong C,
|
||
Pierre G,
|
||
Stuart G,
|
||
Hancox JC</span><br />
|
||
<span class="medgenPMjournal">Ann Noninvasive Electrocardiol</span>
|
||
2023 Nov;28(6):e13077.
|
||
Epub 2023 Sep 1
|
||
doi: 10.1111/anec.13077.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37658577" target="_blank">37658577</a><a href="/pmc/articles/PMC10646383" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35689132">Clinical outcomes of implantable cardioverter-defibrillator therapy in noncompaction cardiomyopathy: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tukker M,
|
||
Schinkel AFL,
|
||
Dereci A,
|
||
Caliskan K</span><br />
|
||
<span class="medgenPMjournal">Heart Fail Rev</span>
|
||
2023 Jan;28(1):241-248.
|
||
Epub 2022 Jun 10
|
||
doi: 10.1007/s10741-022-10250-w.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35689132" target="_blank">35689132</a><a href="/pmc/articles/PMC9902401" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34918480">A proposed strategy for anticoagulation therapy in noncompaction cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chimenti C,
|
||
Lavalle C,
|
||
Magnocavallo M,
|
||
Alfarano M,
|
||
Mariani MV,
|
||
Bernardini F,
|
||
Della Rocca DG,
|
||
Galardo G,
|
||
Severino P,
|
||
Di Lullo L,
|
||
Miraldi F,
|
||
Fedele F,
|
||
Frustaci A</span><br />
|
||
<span class="medgenPMjournal">ESC Heart Fail</span>
|
||
2022 Feb;9(1):241-250.
|
||
Epub 2021 Dec 16
|
||
doi: 10.1002/ehf2.13694.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34918480" target="_blank">34918480</a><a href="/pmc/articles/PMC8788052" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28878579">Left Ventricular Noncompaction Cardiomyopathy Presenting with Heart Failure in a 35-Year-Old Man.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Papadopoulos K,
|
||
Petrou PM,
|
||
Michaelides D</span><br />
|
||
<span class="medgenPMjournal">Tex Heart Inst J</span>
|
||
2017 Aug;44(4):260-263.
|
||
Epub 2017 Aug 1
|
||
doi: 10.14503/THIJ-15-5371.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28878579" target="_blank">28878579</a><a href="/pmc/articles/PMC5577951" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23411903">Noncompaction cardiomyopathy manifesting as retinal artery occlusion.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jin-Poi T,
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Shatriah I,
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<div class="nl"><a target="_blank" href="/pubmed/33731536">Poor Myocardial Compaction in a Patient with Recessive MYL2 Myopathy.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Tamamitsu AM,
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<div class="nl"><a target="_blank" href="/pubmed/30848673">Dilated cardiomyopathy in a pediatric population: etiology and outcome predictors - a single-center experience.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Ciuca C,
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Ragni L,
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Hasan T,
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Balducci A,
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2019 Mar;15(2):95-107.
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<div class="nl"><a target="_blank" href="/pubmed/29447731">Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">van Waning JI,
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Caliskan K,
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Hoedemaekers YM,
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van Spaendonck-Zwarts KY,
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Baas AF,
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Boekholdt SM,
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van Melle JP,
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Teske AJ,
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Asselbergs FW,
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Backx APCM,
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du Marchie Sarvaas GJ,
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Dalinghaus M,
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Breur JMPJ,
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Linschoten MPM,
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Verlooij LA,
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Kardys I,
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Dooijes D,
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Lekanne Deprez RH,
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IJpma AS,
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van den Berg MP,
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Hofstra RMW,
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van Slegtenhorst MA,
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Jongbloed JDH,
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2018 Feb 20;71(7):711-722.
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<span class="bold">PMID: </span><a href="/pubmed/29447731" target="_blank">29447731</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/29221698">Undulating Clinical Course of Noncompaction Cardiomyopathy.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Dolader P,
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Gran F,
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Giralt G,
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Ferrer Q,
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Rosés-Noguer F,
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Albert DC</span><br />
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<span class="medgenPMjournal">Rev Esp Cardiol (Engl Ed)</span>
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2018 Dec;71(12):1077-1079.
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Epub 2017 Dec 6
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<span class="bold">PMID: </span><a href="/pubmed/29221698" target="_blank">29221698</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28079110">Left ventricular noncompaction cardiomyopathy: cardiac, neuromuscular, and genetic factors.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Finsterer J,
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Stöllberger C,
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Towbin JA</span><br />
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<span class="medgenPMjournal">Nat Rev Cardiol</span>
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2017 Apr;14(4):224-237.
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Epub 2017 Jan 12
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<span class="bold">PMID: </span><a href="/pubmed/28079110" target="_blank">28079110</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Noncompaction%20cardiomyopathy%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 (88)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/34384546">Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Casas G,
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Limeres J,
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Oristrell G,
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Borregan M,
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Codina-Solà M,
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Sorolla-Romero JA,
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Fernández-Álvarez P,
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González-Carrillo J,
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Guala A,
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La Mura L,
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Soler-Fernández R,
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Sao Avilés A,
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Santos-Mateo JJ,
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Marsal JR,
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Ribera A,
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de la Pompa JL,
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Villacorta E,
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Jiménez-Jáimez J,
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Ripoll-Vera T,
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Bayes-Genis A,
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Garcia-Pinilla JM,
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Palomino-Doza J,
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Tiron C,
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Pontone G,
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Bogaert J,
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Aquaro GD,
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Gimeno-Blanes JR,
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Zorio E,
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Garcia-Pavia P,
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Barriales-Villa R,
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Evangelista A,
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Masci PG,
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Ferreira-González I,
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<span class="medgenPMjournal">J Am Coll Cardiol</span>
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2021 Aug 17;78(7):643-662.
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doi: 10.1016/j.jacc.2021.06.016.
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<span class="bold">PMID: </span><a href="/pubmed/34384546" target="_blank">34384546</a></div>
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||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30848673">Dilated cardiomyopathy in a pediatric population: etiology and outcome predictors - a single-center experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ciuca C,
|
||
Ragni L,
|
||
Hasan T,
|
||
Balducci A,
|
||
Angeli E,
|
||
Prandstraller D,
|
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Egidy-Assenza G,
|
||
Donti A,
|
||
Bonvicini M,
|
||
Gargiulo GD</span><br />
|
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<span class="medgenPMjournal">Future Cardiol</span>
|
||
2019 Mar;15(2):95-107.
|
||
Epub 2019 Mar 8
|
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doi: 10.2217/fca-2018-0030.
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||
<span class="bold">PMID: </span><a href="/pubmed/30848673" target="_blank">30848673</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29859913">Improvement of the Diagnosis of Left Ventricular Noncompaction Cardiomyopathy After Analyzing Both Advantages and Disadvantages of Echocardiography and CMRI.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Xu Y,
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Liu X,
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Li H</span><br />
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<span class="medgenPMjournal">Prog Cardiovasc Dis</span>
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2018 Nov-Dec;61(5-6):491-493.
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Epub 2018 May 31
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doi: 10.1016/j.pcad.2018.05.006.
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<span class="bold">PMID: </span><a href="/pubmed/29859913" target="_blank">29859913</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/29447731">Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van Waning JI,
|
||
Caliskan K,
|
||
Hoedemaekers YM,
|
||
van Spaendonck-Zwarts KY,
|
||
Baas AF,
|
||
Boekholdt SM,
|
||
van Melle JP,
|
||
Teske AJ,
|
||
Asselbergs FW,
|
||
Backx APCM,
|
||
du Marchie Sarvaas GJ,
|
||
Dalinghaus M,
|
||
Breur JMPJ,
|
||
Linschoten MPM,
|
||
Verlooij LA,
|
||
Kardys I,
|
||
Dooijes D,
|
||
Lekanne Deprez RH,
|
||
IJpma AS,
|
||
van den Berg MP,
|
||
Hofstra RMW,
|
||
van Slegtenhorst MA,
|
||
Jongbloed JDH,
|
||
Majoor-Krakauer D</span><br />
|
||
<span class="medgenPMjournal">J Am Coll Cardiol</span>
|
||
2018 Feb 20;71(7):711-722.
|
||
doi: 10.1016/j.jacc.2017.12.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29447731" target="_blank">29447731</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27568117">LV Noncompaction Cardiomyopathy or Just a Lot of Trabeculations?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aung N,
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Zemrak F,
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Mohiddin SA,
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Petersen SE</span><br />
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<span class="medgenPMjournal">JACC Cardiovasc Imaging</span>
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2017 Jun;10(6):704-707.
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Epub 2016 Aug 24
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doi: 10.1016/j.jcmg.2016.03.014.
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<span class="bold">PMID: </span><a href="/pubmed/27568117" target="_blank">27568117</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Noncompaction%20cardiomyopathy%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 (64)</a></div></div>
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<div class="portlet_content ln">
|
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<div class="nl"><a target="_blank" href="/pubmed/38684446">Electrophysiological phenotyping of left ventricular noncompaction cardiomyopathy in pediatric populations: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fitzsimons LA,
|
||
Kneeland-Barber DM,
|
||
Hannigan GC,
|
||
Karpe DA,
|
||
Wu L,
|
||
Colon M,
|
||
Randall J,
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||
Tucker KL</span><br />
|
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<span class="medgenPMjournal">Physiol Rep</span>
|
||
2024 May;12(9):e16029.
|
||
doi: 10.14814/phy2.16029.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38684446" target="_blank">38684446</a><a href="/pmc/articles/PMC11058051" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35689132">Clinical outcomes of implantable cardioverter-defibrillator therapy in noncompaction cardiomyopathy: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tukker M,
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Schinkel AFL,
|
||
Dereci A,
|
||
Caliskan K</span><br />
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<span class="medgenPMjournal">Heart Fail Rev</span>
|
||
2023 Jan;28(1):241-248.
|
||
Epub 2022 Jun 10
|
||
doi: 10.1007/s10741-022-10250-w.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35689132" target="_blank">35689132</a><a href="/pmc/articles/PMC9902401" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31771441">Systematic Review of Genotype-Phenotype Correlations in Noncompaction Cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van Waning JI,
|
||
Moesker J,
|
||
Heijsman D,
|
||
Boersma E,
|
||
Majoor-Krakauer D</span><br />
|
||
<span class="medgenPMjournal">J Am Heart Assoc</span>
|
||
2019 Dec 3;8(23):e012993.
|
||
Epub 2019 Nov 27
|
||
doi: 10.1161/JAHA.119.012993.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31771441" target="_blank">31771441</a><a href="/pmc/articles/PMC6912966" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Noncompaction%20cardiomyopathy%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 (3)</a></div></div>
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