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<meta name="keywords" content="C1856184, disease or syndrome, hemi 3 syndrome, hemi-3 syndrome, hemicorporal hypertrophy, hemihyperplasia, hemihyperplasia, isolated, hemihypertrophy, hemihypertrophy, isolated, hhp, ih, isolated hemihyperplasia, isolated hemihypertrophy, 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="Isolated hemihyperplasia is an abnormality of cell proliferation leading to asymmetric overgrowth of one or more regions of the body. The term 'hemihyperplasia' has replaced the term 'hemihypertrophy' to describe accurately the increase in cell number found in these patients. The incidence of isolated hemihyperplasia is estimated to be 1 in 86,000. Idiopathic hemihypertrophy is associated with increased risk of embryonal cancers in childhood, particularly Wilms tumor (194070) (Shuman et al., 2006). Hoyme et al. (1998) provided an anatomic classification of hemihyperplasia: complex hemihyperplasia is involvement of half of the body, including at least 1 arm and 1 leg; affected parts may be contralateral or ipsilateral. Simple hemihyperplasia is involvement of a single limb. See also facial hemihyperplasia (133900). Although isolated hemihyperplasia is a distinct clinical entity, it can also occur as a feature of overgrowth syndromes, including Beckwith-Wiedemann syndrome (BWS; 130650), neurofibromatosis (NF1; 162200), Proteus syndrome (176920), and Klippel-Trenaunay-Weber syndrome (149000) (Shuman et al., 2006)." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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||
UID=383853
|
||
ConceptID=C1856184
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Isolated hemihyperplasia<span class="h1sub">(IH)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>383853</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.">C1856184</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>Hemi 3 syndrome; IH</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0009331" target="_blank">MONDO:0009331</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/235000" target="_blank">235000</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=2128">ORPHA2128</a></td></tr></tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
|
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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>
|
||
<div class="portlet_content ln">Isolated hemihyperplasia is an abnormality of cell proliferation leading to asymmetric overgrowth of one or more regions of the body. The term 'hemihyperplasia' has replaced the term 'hemihypertrophy' to describe accurately the increase in cell number found in these patients. The incidence of isolated hemihyperplasia is estimated to be 1 in 86,000. Idiopathic hemihypertrophy is associated with increased risk of embryonal cancers in childhood, particularly Wilms tumor (194070) (Shuman et al., 2006). Hoyme et al. (1998) provided an anatomic classification of hemihyperplasia: complex hemihyperplasia is involvement of half of the body, including at least 1 arm and 1 leg; affected parts may be contralateral or ipsilateral. Simple hemihyperplasia is involvement of a single limb. See also facial hemihyperplasia (133900). Although isolated hemihyperplasia is a distinct clinical entity, it can also occur as a feature of overgrowth syndromes, including Beckwith-Wiedemann syndrome (BWS; 130650), neurofibromatosis (NF1; 162200), Proteus syndrome (176920), and Klippel-Trenaunay-Weber syndrome (149000) (Shuman et al., 2006). [from <a title="Online Mendelian Inheritance in Man" href="http://www.omim.org" class="defSource" target="_blank">OMIM</a>]</div>
|
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</div>
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<div class="portlet mgSection" id="ID_102">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
|
||
<div class="divPopper rprt" id="clin_45034"><div><strong>Embryonal neoplasm</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>45034</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.">C0027654</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Neoplastic Process</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A usually malignant neoplasm composed of primitive (immature) tissues that resemble fetal tissues. Medulloblastoma, ependymoblastoma, pineoblastoma, and Wilms tumor are representative embryonal neoplasms.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/45034">Feature record</a> | <a href="/medgen?term=%22Embryonal%20neoplasm%22%5BClinical%20Features%5D%20OR%2045034%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_10221"><div><strong>Nephroblastoma</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>10221</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.">C0027708</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Neoplastic Process</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The presence of a nephroblastoma, which is a neoplasm of the kidney that primarily affects children.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/10221">Feature record</a> | <a href="/medgen?term=%22Nephroblastoma%22%5BClinical%20Features%5D%20OR%2010221%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_90701"><div><strong>Hemihypertrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>90701</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.">C0332890</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Overgrowth of only one side of the body.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/90701">Feature record</a> | <a href="/medgen?term=%22Hemihypertrophy%22%5BClinical%20Features%5D%20OR%2090701%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_7538"><div><strong>Myelomeningocele</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>7538</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.">C0025312</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Protrusion of the meninges and portions of the spinal cord through a defect of the vertebral column.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/7538">Feature record</a> | <a href="/medgen?term=%22Myelomeningocele%22%5BClinical%20Features%5D%20OR%207538%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_10044"><div><strong>Intellectual disability, mild</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>10044</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.">C0026106</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Mild intellectual disability is defined as an intelligence quotient (IQ) in the range of 50-69.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/10044">Feature record</a> | <a href="/medgen?term=%22Intellectual%20disability%2C%20mild%22%5BClinical%20Features%5D%20OR%2010044%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_11348"><div><strong>Scoliosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>11348</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.">C0036439</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The presence of an abnormal lateral curvature of the spine.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/11348">Feature record</a> | <a href="/medgen?term=%22Scoliosis%22%5BClinical%20Features%5D%20OR%2011348%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_853739"><div><strong>Skeletal muscle hypertrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>853739</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.">C2265792</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Abnormal increase in muscle size and mass not due to training.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/853739">Feature record</a> | <a href="/medgen?term=%22Skeletal%20muscle%20hypertrophy%22%5BClinical%20Features%5D%20OR%20853739%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite" data-jigconfig="closed: 1"><div class="concept-def"><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().openAll(); return false;">Show all</a><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().closeAll(); return false;">Hide all</a></div><ul><li><span class="TLline">Abnormality of the musculoskeletal system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_11348" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Scoliosis</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_853739" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Skeletal muscle hypertrophy</a></span></li></ul></li><li><span class="TLline">Abnormality of the nervous system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_10044" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, mild</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_7538" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Myelomeningocele</a></span></li></ul></li><li><span class="TLline">Growth abnormality</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_90701" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hemihypertrophy</a></span></li></ul></li><li><span class="TLline">Neoplasm</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_45034" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Embryonal neoplasm</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_10221" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nephroblastoma</a></span></li></ul></li></ul></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_118">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet Rcolor round" title="Research test"><a target="_blank" href="/gtr/tests/?term=C1856184[DISCUI]&test_type=Research&redirect=true" ref="ncbi_uid=383853">R</a></span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=383853" target="_blank" href="/omim/235000">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1294/" ref="ncbi_uid=383853">G</a></span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Isolated hemihyperplasia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/871375" ref="tree=MeSH" title="MedGen record for Abnormality of the face">Abnormality of the face</a></span><ul><li><span class="TLline"><a href="/medgen/6447" ref="tree=MeSH" title="MedGen record for Abnormality of the mouth">Abnormality of the mouth</a></span><ul><li><span class="TLline"><a href="/medgen/1645271" ref="tree=MeSH" title="MedGen record for Abnormal oral morphology">Abnormal oral morphology</a></span><ul><li><span class="TLline"><a href="/medgen/871391" ref="tree=MeSH" title="MedGen record for Abnormal oral cavity morphology">Abnormal oral cavity morphology</a></span><ul><li><span class="TLline"><a href="/medgen/895701" ref="tree=MeSH" title="MedGen record for Abnormal tongue morphology">Abnormal tongue morphology</a></span><ul><li><span class="TLline"><a href="/medgen/44236" ref="tree=MeSH" title="MedGen record for Macroglossia">Macroglossia</a></span><ul><li><span class="matched_ds">Isolated hemihyperplasia</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_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/21446802">Syndromes with focal overgrowth in infancy: diagnostic approach and surgical treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mirastschijski U,
|
||
Altmann S,
|
||
Lenz-Scharf O,
|
||
Muschke P,
|
||
Schneider W</span><br />
|
||
<span class="medgenPMjournal">J Plast Surg Hand Surg</span>
|
||
2012 Feb;46(1):45-8.
|
||
Epub 2010 Sep 6
|
||
doi: 10.3109/02844310902957728.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21446802" target="_blank">21446802</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19367194">Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Clericuzio CL,
|
||
Martin RA</span><br />
|
||
<span class="medgenPMjournal">Genet Med</span>
|
||
2009 Mar;11(3):220-2.
|
||
doi: 10.1097/GIM.0b013e31819436cf.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19367194" target="_blank">19367194</a><a href="/pmc/articles/PMC3111026" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22isolated%20hemihyperplasia%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 (2)</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/34627330">Prospective study of epigenetic alterations responsible for isolated hemihyperplasia/hemihypoplasia and their association with leg length discrepancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shin CH,
|
||
Lim C,
|
||
Kim HY,
|
||
Yoo WJ,
|
||
Cho TJ,
|
||
Choi IH,
|
||
Ko JM</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2021 Oct 9;16(1):418.
|
||
doi: 10.1186/s13023-021-02042-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34627330" target="_blank">34627330</a><a href="/pmc/articles/PMC8501601" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19367194">Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Clericuzio CL,
|
||
Martin RA</span><br />
|
||
<span class="medgenPMjournal">Genet Med</span>
|
||
2009 Mar;11(3):220-2.
|
||
doi: 10.1097/GIM.0b013e31819436cf.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19367194" target="_blank">19367194</a><a href="/pmc/articles/PMC3111026" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16925531">Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: a critical review of the evidence and suggested guidelines for local practice.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tan TY,
|
||
Amor DJ</span><br />
|
||
<span class="medgenPMjournal">J Paediatr Child Health</span>
|
||
2006 Sep;42(9):486-90.
|
||
doi: 10.1111/j.1440-1754.2006.00908.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16925531" target="_blank">16925531</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16877856">Hemihyperplasia syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dalal AB,
|
||
Phadke SR,
|
||
Pradhan M,
|
||
Sharda S</span><br />
|
||
<span class="medgenPMjournal">Indian J Pediatr</span>
|
||
2006 Jul;73(7):609-15.
|
||
doi: 10.1007/BF02759927.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16877856" target="_blank">16877856</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9781907">Isolated hemihyperplasia (hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hoyme HE,
|
||
Seaver LH,
|
||
Jones KL,
|
||
Procopio F,
|
||
Crooks W,
|
||
Feingold M</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet</span>
|
||
1998 Oct 2;79(4):274-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9781907" target="_blank">9781907</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Isolated%20hemihyperplasia%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 (16)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34627330">Prospective study of epigenetic alterations responsible for isolated hemihyperplasia/hemihypoplasia and their association with leg length discrepancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shin CH,
|
||
Lim C,
|
||
Kim HY,
|
||
Yoo WJ,
|
||
Cho TJ,
|
||
Choi IH,
|
||
Ko JM</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2021 Oct 9;16(1):418.
|
||
doi: 10.1186/s13023-021-02042-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34627330" target="_blank">34627330</a><a href="/pmc/articles/PMC8501601" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19367194">Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Clericuzio CL,
|
||
Martin RA</span><br />
|
||
<span class="medgenPMjournal">Genet Med</span>
|
||
2009 Mar;11(3):220-2.
|
||
doi: 10.1097/GIM.0b013e31819436cf.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19367194" target="_blank">19367194</a><a href="/pmc/articles/PMC3111026" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16925531">Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: a critical review of the evidence and suggested guidelines for local practice.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tan TY,
|
||
Amor DJ</span><br />
|
||
<span class="medgenPMjournal">J Paediatr Child Health</span>
|
||
2006 Sep;42(9):486-90.
|
||
doi: 10.1111/j.1440-1754.2006.00908.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16925531" target="_blank">16925531</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16877856">Hemihyperplasia syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dalal AB,
|
||
Phadke SR,
|
||
Pradhan M,
|
||
Sharda S</span><br />
|
||
<span class="medgenPMjournal">Indian J Pediatr</span>
|
||
2006 Jul;73(7):609-15.
|
||
doi: 10.1007/BF02759927.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16877856" target="_blank">16877856</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12972772">Bilateral retinal telangiectasia and exudative retinopathy associated with isolated hemihyperplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Haritoglou C,
|
||
Schmidt H,
|
||
Rudolph G,
|
||
Ulbig MW</span><br />
|
||
<span class="medgenPMjournal">Retina</span>
|
||
2003 Aug;23(4):549-52.
|
||
doi: 10.1097/00006982-200308000-00020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12972772" target="_blank">12972772</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Isolated%20hemihyperplasia%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 (14)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/16770802">Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shuman C,
|
||
Smith AC,
|
||
Steele L,
|
||
Ray PN,
|
||
Clericuzio C,
|
||
Zackai E,
|
||
Parisi MA,
|
||
Meadows AT,
|
||
Kelly T,
|
||
Tichauer D,
|
||
Squire JA,
|
||
Sadowski P,
|
||
Weksberg R</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2006 Jul 15;140(14):1497-503.
|
||
doi: 10.1002/ajmg.a.31323.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16770802" target="_blank">16770802</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Isolated%20hemihyperplasia%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34627330">Prospective study of epigenetic alterations responsible for isolated hemihyperplasia/hemihypoplasia and their association with leg length discrepancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shin CH,
|
||
Lim C,
|
||
Kim HY,
|
||
Yoo WJ,
|
||
Cho TJ,
|
||
Choi IH,
|
||
Ko JM</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2021 Oct 9;16(1):418.
|
||
doi: 10.1186/s13023-021-02042-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34627330" target="_blank">34627330</a><a href="/pmc/articles/PMC8501601" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25804021">Results of fifteen-year follow-up from a single center: findings and risks for tumor development in isolated hemihyperplasia cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Atik T,
|
||
Cogulu O,
|
||
Ozkinay F</span><br />
|
||
<span class="medgenPMjournal">Genet Couns</span>
|
||
2014;25(4):417-21.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25804021" target="_blank">25804021</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22411341">Incidence of abdominal tumors in syndromic and idiopathic hemihypertrophy/isolated hemihyperplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dempsey-Robertson M,
|
||
Wilkes D,
|
||
Stall A,
|
||
Bush P</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Orthop</span>
|
||
2012 Apr-May;32(3):322-6.
|
||
doi: 10.1097/BPO.0b013e3182471b04.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22411341" target="_blank">22411341</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21446802">Syndromes with focal overgrowth in infancy: diagnostic approach and surgical treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mirastschijski U,
|
||
Altmann S,
|
||
Lenz-Scharf O,
|
||
Muschke P,
|
||
Schneider W</span><br />
|
||
<span class="medgenPMjournal">J Plast Surg Hand Surg</span>
|
||
2012 Feb;46(1):45-8.
|
||
Epub 2010 Sep 6
|
||
doi: 10.3109/02844310902957728.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21446802" target="_blank">21446802</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18571544">Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bliek J,
|
||
Maas S,
|
||
Alders M,
|
||
Merks JH,
|
||
Mannens M</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2008 Jul;153(1):95-100.
|
||
Epub 2008 Mar 7
|
||
doi: 10.1016/j.jpeds.2007.12.022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18571544" target="_blank">18571544</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Isolated%20hemihyperplasia%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 (5)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36374059">Isolated lateralized overgrowth: clinical, radiological, and auxological characteristics of a single-site cohort of 76 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Romaris MJ,
|
||
Caino S,
|
||
Adamo P,
|
||
Fano V</span><br />
|
||
<span class="medgenPMjournal">Arch Argent Pediatr</span>
|
||
2022 Dec;120(6):405-414.
|
||
Epub 2022 Oct 25
|
||
doi: 10.5546/aap.2022.eng.405.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36374059" target="_blank">36374059</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34627330">Prospective study of epigenetic alterations responsible for isolated hemihyperplasia/hemihypoplasia and their association with leg length discrepancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shin CH,
|
||
Lim C,
|
||
Kim HY,
|
||
Yoo WJ,
|
||
Cho TJ,
|
||
Choi IH,
|
||
Ko JM</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2021 Oct 9;16(1):418.
|
||
doi: 10.1186/s13023-021-02042-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34627330" target="_blank">34627330</a><a href="/pmc/articles/PMC8501601" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20503313">CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Romanelli V,
|
||
Belinchón A,
|
||
Benito-Sanz S,
|
||
Martínez-Glez V,
|
||
Gracia-Bouthelier R,
|
||
Heath KE,
|
||
Campos-Barros A,
|
||
García-Miñaur S,
|
||
Fernandez L,
|
||
Meneses H,
|
||
López-Siguero JP,
|
||
Guillén-Navarro E,
|
||
Gómez-Puertas P,
|
||
Wesselink JJ,
|
||
Mercado G,
|
||
Esteban-Marfil V,
|
||
Palomo R,
|
||
Mena R,
|
||
Sánchez A,
|
||
Del Campo M,
|
||
Lapunzina P</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2010 Jun;152A(6):1390-7.
|
||
doi: 10.1002/ajmg.a.33453.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20503313" target="_blank">20503313</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18571544">Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bliek J,
|
||
Maas S,
|
||
Alders M,
|
||
Merks JH,
|
||
Mannens M</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2008 Jul;153(1):95-100.
|
||
Epub 2008 Mar 7
|
||
doi: 10.1016/j.jpeds.2007.12.022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18571544" target="_blank">18571544</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16925531">Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: a critical review of the evidence and suggested guidelines for local practice.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tan TY,
|
||
Amor DJ</span><br />
|
||
<span class="medgenPMjournal">J Paediatr Child Health</span>
|
||
2006 Sep;42(9):486-90.
|
||
doi: 10.1111/j.1440-1754.2006.00908.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16925531" target="_blank">16925531</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Isolated%20hemihyperplasia%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 (6)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
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||
<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_content ln"><ul id="my-toc"></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Genetic_Testing_Registry">Genetic Testing Registry</h1><a sid="106" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C1856184%5bDISCUI%5d&test_type=Research" target="_blank">Research (1)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C1856184%5bDISCUI%5d" target="_blank">See all (1)</a></total></li>
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|
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|
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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://www.omim.org/search?index=entry&start=1&limit=10&sort=score%20desc&field=number&search=235000" target="_blank">OMIM</a></li><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=2128" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Isolated%20hemihyperplasia" 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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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22isolated%20hemihyperplasia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Isolated%20hemihyperplasia%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_head mgSectionHead ui-widget-header"><h1 class="nl" id="Molecular_resources">Molecular resources</h1><a sid="115" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://catalog.coriell.org/Search?q=235000" target="_blank">Coriell Institute for Medical Research</a></li></ul></div>
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||
<div class="portlet_content ln"><ul><li><a href="http://www.diseaseinfosearch.org/Hemi+3+syndrome/3276" target="_blank">Genetic Alliance</a></li><li><a href="https://www.malacards.org/card/hemihyperplasia_isolated" target="_blank">MalaCards</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Isolated%20hemihyperplasia" target="_blank">MedlinePlus</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/2630/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
|
||
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|
||
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|
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<li>
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<a href="/pubmed/20301471" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=3" target="_blank"><span class="gene_reviews">GeneReviews</span></a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed/clinical?term=Isolated%20hemihyperplasia" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=3" target="_blank">PubMed Clinical Queries</a>
|
||
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||
<li>
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<a href="/pubmed?term=Isolated%20hemihyperplasia%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=3&linkpostotal=3" target="_blank">Reviews in PubMed</a>
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<h3>Related information</h3>
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<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/gtr/tests?term=C1856184[DISCUI]" ref="log$=recordlinks">GTR</a>
|
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<div class="brieflinkpop offscreen_noflow">Related information in GTR</div>
|
||
</li>
|
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<li class="brieflinkpopper">
|
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<a class="brieflinkpopperctrl" href="/gtr/tests?term=C1856184[DISCUI]&test_type=Research" ref="log$=recordlinks">GTR(Research)</a>
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<div class="brieflinkpop offscreen_noflow">Research tests in GTR</div>
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<a class="brieflinkpopperctrl" href="/mesh?LinkName=medgen_mesh&from_uid=383853" ref="log$=recordlinks">MeSH</a>
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<div class="brieflinkpop offscreen_noflow">Related Medical Subject Headings</div>
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<a class="brieflinkpopperctrl" href="/omim?LinkName=medgen_omim&from_uid=383853" ref="log$=recordlinks">OMIM</a>
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<div class="brieflinkpop offscreen_noflow">Related records in OMIM</div>
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=383853" ref="log$=recordlinks">PMC Articles</a>
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<div class="brieflinkpop offscreen_noflow">Related information in PubMed Central Links</div>
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=383853" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_bookshelf_cited&from_uid=383853" ref="log$=recordlinks">PubMed (Bookshelf cited)</a>
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<div class="brieflinkpop offscreen_noflow">Links to PubMed based on citations in GeneReviews and Medical Genetics Summaries</div>
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_genereviews&from_uid=383853" ref="log$=recordlinks">PubMed (GeneReviews)</a>
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<div class="brieflinkpop offscreen_noflow">GeneReviews in PubMed</div>
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</li>
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<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_omim&from_uid=383853" ref="log$=recordlinks">PubMed (OMIM)</a>
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||
<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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