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<meta name="keywords" content="C3178805, disease or syndrome, heterotaxia, heterotaxia syndrome, heterotaxy syndrome, heterotaxy syndromes, heterotaxy, visceral, incomplete situs inversus, lateralization defect, partial situs inversus, situs ambiguous, situs ambiguus, syndrome, heterotaxy, syndromes, heterotaxy, visceral heterotaxy, 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="Heterotaxy syndrome is a condition in which the internal organs are abnormally arranged in the chest and abdomen. The term "heterotaxy" is from the Greek words "heteros," meaning "other than," and "taxis," meaning "arrangement." Individuals with this condition have complex birth defects affecting the heart, lungs, liver, spleen, intestines, and other organs.\n\nIn the normal body, most of the organs in the chest and abdomen have a particular location on the right or left side. For example, the heart, spleen, and pancreas are on the left side of the body, and most of the liver is on the right. This normal arrangement of the organs is known as "situs solitus." Rarely, the orientation of the internal organs is completely flipped from right to left, a situation known as "situs inversus." This mirror-image orientation usually does not cause any health problems, unless it occurs as part of a syndrome affecting other parts of the body. Heterotaxy syndrome is an arrangement of internal organs somewhere between situs solitus and situs inversus; this condition is also known as "situs ambiguus." Unlike situs inversus, the abnormal arrangement of organs in heterotaxy syndrome often causes serious health problems.\n\nHeterotaxy syndrome can alter the structure of the heart, including the attachment of the large blood vessels that carry blood to and from the rest of the body. It can also affect the structure of the lungs, such as the number of lobes in each lung and the length of the tubes (called bronchi) that lead from the windpipe to the lungs. In the abdomen, the condition can cause a person to have no spleen (asplenia) or multiple small, poorly functioning spleens (polysplenia). The liver may lie across the middle of the body instead of being in its normal position to the right of the stomach. Some affected individuals also have intestinal malrotation, which is an abnormal twisting of the intestines that occurs in the early stages of development before birth.\n\nDepending on the organs involved, signs and symptoms of heterotaxy syndrome can include a bluish appearance of the skin or lips (cyanosis, which is due to a shortage of oxygen), breathing difficulties, an increased risk of infections, and problems with digesting food. The most serious complications are generally caused by critical congenital heart disease, a group of complex heart defects that are present from birth. Biliary atresia, a problem with the bile ducts in the liver, can also cause severe health problems in infancy.\n\nThe severity of heterotaxy syndrome varies depending on the specific abnormalities involved. Some affected individuals have only mild health problems related to the condition. At the other end of the spectrum, heterotaxy syndrome can be life-threatening in infancy or childhood, even with treatment." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=465273
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ConceptID=C3178805
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Visceral heterotaxy</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>465273</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:">C3178805</span></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>Heterotaxia; Heterotaxy syndrome</td></tr>
|
||
<tr><td>Modes of inheritance:</td>
|
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<td>
|
||
<div class="divPopper rprt" id="moi_141025"><div><strong>Autosomal recessive inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141025</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.">C0441748</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Intellectual Product</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).</div></div>
|
||
<div class="divPopper rprt" id="moi_141047"><div><strong>Autosomal dominant inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141047</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.">C0443147</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Intellectual Product</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.</div></div>
|
||
<div class="divPopper rprt" id="moi_375779"><div><strong>X-linked recessive inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>375779</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.">C1845977</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for recessive traits related to a gene encoded on the X chromosome. In the context of medical genetics, X-linked recessive disorders manifest in males (who have one copy of the X chromosome and are thus hemizygotes), but generally not in female heterozygotes who have one mutant and one normal allele.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/375779">This record</a></div></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_141025" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive inheritance</a><span> (Orphanet)</span></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_141047" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant inheritance</a><span> (Orphanet)</span></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_375779" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">X-linked recessive inheritance</a><span> (Orphanet)</span></div></td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0018677" target="_blank">MONDO:0018677</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span> Phenotypic series:</td>
|
||
<td><a href="https://omim.org/phenotypicSeries/PS306955" target="_blank">PS306955</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=450">ORPHA450</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">Heterotaxy syndrome is a condition in which the internal organs are abnormally arranged in the chest and abdomen. The term "heterotaxy" is from the Greek words "heteros," meaning "other than," and "taxis," meaning "arrangement." Individuals with this condition have complex birth defects affecting the heart, lungs, liver, spleen, intestines, and other organs.<br /><br />In the normal body, most of the organs in the chest and abdomen have a particular location on the right or left side. For example, the heart, spleen, and pancreas are on the left side of the body, and most of the liver is on the right. This normal arrangement of the organs is known as "situs solitus." Rarely, the orientation of the internal organs is completely flipped from right to left, a situation known as "situs inversus." This mirror-image orientation usually does not cause any health problems, unless it occurs as part of a syndrome affecting other parts of the body. Heterotaxy syndrome is an arrangement of internal organs somewhere between situs solitus and situs inversus; this condition is also known as "situs ambiguus." Unlike situs inversus, the abnormal arrangement of organs in heterotaxy syndrome often causes serious health problems.<br /><br />Heterotaxy syndrome can alter the structure of the heart, including the attachment of the large blood vessels that carry blood to and from the rest of the body. It can also affect the structure of the lungs, such as the number of lobes in each lung and the length of the tubes (called bronchi) that lead from the windpipe to the lungs. In the abdomen, the condition can cause a person to have no spleen (asplenia) or multiple small, poorly functioning spleens (polysplenia). The liver may lie across the middle of the body instead of being in its normal position to the right of the stomach. Some affected individuals also have intestinal malrotation, which is an abnormal twisting of the intestines that occurs in the early stages of development before birth.<br /><br />Depending on the organs involved, signs and symptoms of heterotaxy syndrome can include a bluish appearance of the skin or lips (cyanosis, which is due to a shortage of oxygen), breathing difficulties, an increased risk of infections, and problems with digesting food. The most serious complications are generally caused by critical congenital heart disease, a group of complex heart defects that are present from birth. Biliary atresia, a problem with the bile ducts in the liver, can also cause severe health problems in infancy.<br /><br />The severity of heterotaxy syndrome varies depending on the specific abnormalities involved. Some affected individuals have only mild health problems related to the condition. At the other end of the spectrum, heterotaxy syndrome can be life-threatening in infancy or childhood, even with treatment. [from <a title="MedlinePlus Genetics" href="https://medlineplus.gov/genetics/" class="defSource" target="_blank">MedlinePlus Genetics</a>]</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>
|
||
<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><li><a href="#tabORDO">Orphanet</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 Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C3178805[DISCUI]&test_type=Clinical" ref="ncbi_uid=465273">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=465273" ref="ncbi_uid=465273">V</a></span></span><span class="TLline">Visceral heterotaxy</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/232130" ref="tree=MeSH" title="MedGen record for Disorder by Site">Disorder by Site</a></span><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="matched_ds">Visceral heterotaxy</span><ul><li><span class="TLline"><a href="/medgen/4255" ref="tree=MeSH" title="MedGen record for Dextrocardia">Dextrocardia</a></span></li><li><span class="TLline"><a href="/medgen/75620" ref="tree=MeSH" title="MedGen record for Heterotaxy">Heterotaxy</a></span><ul><li><span class="TLline"><a href="/medgen/868855" ref="tree=MeSH" title="MedGen record for Abnormality of abdominal situs">Abnormality of abdominal situs</a></span><ul><li><span class="TLline"><a href="/medgen/1622585" ref="tree=MeSH" title="MedGen record for Abdominal situs ambiguus">Abdominal situs ambiguus</a></span></li><li><span class="TLline"><a href="/medgen/52359" ref="tree=MeSH" title="MedGen record for Abdominal situs inversus">Abdominal situs inversus</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1634559" ref="tree=MeSH" title="MedGen record for Isomerism">Isomerism</a></span><ul><li><span class="TLline"><a href="/medgen/1618562" ref="tree=MeSH" title="MedGen record for Bronchial isomerism">Bronchial isomerism</a></span></li><li><span class="TLline"><a href="/medgen/1640720" ref="tree=MeSH" title="MedGen record for Left Isomerism">Left Isomerism</a></span></li><li><span class="TLline"><a href="/medgen/64222" ref="tree=MeSH" title="MedGen record for Right isomerism">Right isomerism</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/465274" ref="tree=MeSH" title="MedGen record for Right atrial isomerism">Right atrial isomerism</a></span></li><li><span class="TLline"><a href="/medgen/1642262" ref="tree=MeSH" title="MedGen record for Situs inversus">Situs inversus</a></span></li><li><span class="TLline"><a href="/medgen/7331" ref="tree=MeSH" title="MedGen record for Situs inversus with levocardia">Situs inversus with levocardia</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div><div id="tabORDO">Follow <a target="_blank" href="http://www.orpha.net/consor/cgi-bin/Disease_Classif.php?lng=EN&data_id=156&PatId=8556&search=Disease_Classif_Simple&new=1" class="ital bold">this link</a> to review classifications for <span class="ital">Visceral heterotaxy</span> in Orphanet.</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/35355279">Prenatal diagnosis of hepatic interruption of the inferior vena cava with azygos/hemiazygos continuation without structural heart defects: A case series.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Babaoğlu K,
|
||
Doğan Y,
|
||
Başar EZ,
|
||
Usta E</span><br />
|
||
<span class="medgenPMjournal">J Clin Ultrasound</span>
|
||
2022 Jul;50(6):795-802.
|
||
Epub 2022 Mar 30
|
||
doi: 10.1002/jcu.23209.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35355279" target="_blank">35355279</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23035047">Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Saunders CJ,
|
||
Miller NA,
|
||
Soden SE,
|
||
Dinwiddie DL,
|
||
Noll A,
|
||
Alnadi NA,
|
||
Andraws N,
|
||
Patterson ML,
|
||
Krivohlavek LA,
|
||
Fellis J,
|
||
Humphray S,
|
||
Saffrey P,
|
||
Kingsbury Z,
|
||
Weir JC,
|
||
Betley J,
|
||
Grocock RJ,
|
||
Margulies EH,
|
||
Farrow EG,
|
||
Artman M,
|
||
Safina NP,
|
||
Petrikin JE,
|
||
Hall KP,
|
||
Kingsmore SF</span><br />
|
||
<span class="medgenPMjournal">Sci Transl Med</span>
|
||
2012 Oct 3;4(154):154ra135.
|
||
doi: 10.1126/scitranslmed.3004041.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23035047" target="_blank">23035047</a><a href="/pmc/articles/PMC4283791" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22visceral%20heterotaxy%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/38441284">Correlation between COVID-19 infection and fetal situs inversus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Qiu S,
|
||
Wu S,
|
||
Yin R,
|
||
Wang B,
|
||
Wu H</span><br />
|
||
<span class="medgenPMjournal">Birth Defects Res</span>
|
||
2024 Mar;116(3):e2324.
|
||
doi: 10.1002/bdr2.2324.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38441284" target="_blank">38441284</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35355279">Prenatal diagnosis of hepatic interruption of the inferior vena cava with azygos/hemiazygos continuation without structural heart defects: A case series.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Babaoğlu K,
|
||
Doğan Y,
|
||
Başar EZ,
|
||
Usta E</span><br />
|
||
<span class="medgenPMjournal">J Clin Ultrasound</span>
|
||
2022 Jul;50(6):795-802.
|
||
Epub 2022 Mar 30
|
||
doi: 10.1002/jcu.23209.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35355279" target="_blank">35355279</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22726404">Visceral heterotaxy in the developing world.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Changlani DK,
|
||
Kotecha M,
|
||
Changlani TD,
|
||
Varghese R,
|
||
Kumar RS</span><br />
|
||
<span class="medgenPMjournal">Heart Lung Circ</span>
|
||
2012 Sep;21(9):598-605.
|
||
Epub 2012 Jun 20
|
||
doi: 10.1016/j.hlc.2012.05.739.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22726404" target="_blank">22726404</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21233261">Experience with bidirectional cavopulmonary anastomosis and modified Fontan operation in patients with single ventricle and concomitant visceral heterotaxy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yurlov IA,
|
||
Podzolkov VP,
|
||
Zelenikin MM,
|
||
Kovalev DV,
|
||
Babaev GK,
|
||
Putiato NA,
|
||
Zaets SB</span><br />
|
||
<span class="medgenPMjournal">Interact Cardiovasc Thorac Surg</span>
|
||
2011 Apr;12(4):563-8.
|
||
Epub 2011 Jan 13
|
||
doi: 10.1510/icvts.2010.253567.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21233261" target="_blank">21233261</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18039396">The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jacobs JP,
|
||
Anderson RH,
|
||
Weinberg PM,
|
||
Walters HL 3rd,
|
||
Tchervenkov CI,
|
||
Del Duca D,
|
||
Franklin RC,
|
||
Aiello VD,
|
||
Béland MJ,
|
||
Colan SD,
|
||
Gaynor JW,
|
||
Krogmann ON,
|
||
Kurosawa H,
|
||
Maruszewski B,
|
||
Stellin G,
|
||
Elliott MJ</span><br />
|
||
<span class="medgenPMjournal">Cardiol Young</span>
|
||
2007 Sep;17 Suppl 2:1-28.
|
||
doi: 10.1017/S1047951107001138.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18039396" target="_blank">18039396</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Visceral%20heterotaxy%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 (22)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29559246">Intrahepatic cholangiocarcinoma after Fontan procedure in an adult with visceral heterotaxy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang D,
|
||
Marshall D,
|
||
Veldtman G,
|
||
Gupta A,
|
||
Trout AT,
|
||
Villafane J,
|
||
Bove K</span><br />
|
||
<span class="medgenPMjournal">Pathol Res Pract</span>
|
||
2018 Jun;214(6):914-918.
|
||
Epub 2018 Mar 15
|
||
doi: 10.1016/j.prp.2018.03.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29559246" target="_blank">29559246</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25829475">Slow pathway ablation in abdominal visceral heterotaxy with azygos continuation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hu H,
|
||
Li J,
|
||
Cui K</span><br />
|
||
<span class="medgenPMjournal">Europace</span>
|
||
2016 Jan;18(1):56.
|
||
Epub 2015 Mar 31
|
||
doi: 10.1093/europace/euv035.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25829475" target="_blank">25829475</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22843201">Regression of pulmonary vascular disease after therapy of Abernethy malformation in visceral heterotaxy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raghuram KA,
|
||
Bijulal S,
|
||
Krishnamoorthy KM,
|
||
Tharakan JA</span><br />
|
||
<span class="medgenPMjournal">Pediatr Cardiol</span>
|
||
2013;34(8):1882-5.
|
||
Epub 2012 Jul 28
|
||
doi: 10.1007/s00246-012-0428-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22843201" target="_blank">22843201</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22411653">Visceral heterotaxy and malrotation in a neonate.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">MacDonald A,
|
||
Johal NS,
|
||
Haddad M,
|
||
Choudhry MS</span><br />
|
||
<span class="medgenPMjournal">Br J Hosp Med (Lond)</span>
|
||
2012 Mar;73(3):173.
|
||
doi: 10.12968/hmed.2012.73.3.173.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22411653" target="_blank">22411653</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18039397">Controversies, genetics, diagnostic assessment, and outcomes relating to the heterotaxy syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cohen MS,
|
||
Anderson RH,
|
||
Cohen MI,
|
||
Atz AM,
|
||
Fogel M,
|
||
Gruber PJ,
|
||
Lopez L,
|
||
Rome JJ,
|
||
Weinberg PM</span><br />
|
||
<span class="medgenPMjournal">Cardiol Young</span>
|
||
2007 Sep;17 Suppl 2:29-43.
|
||
doi: 10.1017/S104795110700114X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18039397" target="_blank">18039397</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Visceral%20heterotaxy%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 (33)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34814109">Case Report: Cerebral Phaeohyphomycosis Due to Chaetomium strumarium in a Child with Visceral Heterotaxy Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cárdenas Del Castillo B,
|
||
Bejarano JIC,
|
||
DeLaGarza-Pineda O,
|
||
Ruiz JAA,
|
||
Villanueva Lozano H,
|
||
Treviño-Rangel RJ,
|
||
González M G,
|
||
García Martínez JM</span><br />
|
||
<span class="medgenPMjournal">Am J Trop Med Hyg</span>
|
||
2021 Nov 22;106(2):574-577.
|
||
doi: 10.4269/ajtmh.21-0277.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34814109" target="_blank">34814109</a><a href="/pmc/articles/PMC8832948" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29559246">Intrahepatic cholangiocarcinoma after Fontan procedure in an adult with visceral heterotaxy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang D,
|
||
Marshall D,
|
||
Veldtman G,
|
||
Gupta A,
|
||
Trout AT,
|
||
Villafane J,
|
||
Bove K</span><br />
|
||
<span class="medgenPMjournal">Pathol Res Pract</span>
|
||
2018 Jun;214(6):914-918.
|
||
Epub 2018 Mar 15
|
||
doi: 10.1016/j.prp.2018.03.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29559246" target="_blank">29559246</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22843201">Regression of pulmonary vascular disease after therapy of Abernethy malformation in visceral heterotaxy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raghuram KA,
|
||
Bijulal S,
|
||
Krishnamoorthy KM,
|
||
Tharakan JA</span><br />
|
||
<span class="medgenPMjournal">Pediatr Cardiol</span>
|
||
2013;34(8):1882-5.
|
||
Epub 2012 Jul 28
|
||
doi: 10.1007/s00246-012-0428-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22843201" target="_blank">22843201</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22726404">Visceral heterotaxy in the developing world.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Changlani DK,
|
||
Kotecha M,
|
||
Changlani TD,
|
||
Varghese R,
|
||
Kumar RS</span><br />
|
||
<span class="medgenPMjournal">Heart Lung Circ</span>
|
||
2012 Sep;21(9):598-605.
|
||
Epub 2012 Jun 20
|
||
doi: 10.1016/j.hlc.2012.05.739.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22726404" target="_blank">22726404</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11005603">Omental flap for mediastinitis after median sternotomy in asplenia syndrome and gut malrotation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aeba R,
|
||
Katogi T,
|
||
Moro K,
|
||
Kawada S</span><br />
|
||
<span class="medgenPMjournal">Thorac Cardiovasc Surg</span>
|
||
2000 Aug;48(4):243-4.
|
||
doi: 10.1055/s-2000-6891.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11005603" target="_blank">11005603</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Visceral%20heterotaxy%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 (9)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35355279">Prenatal diagnosis of hepatic interruption of the inferior vena cava with azygos/hemiazygos continuation without structural heart defects: A case series.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Babaoğlu K,
|
||
Doğan Y,
|
||
Başar EZ,
|
||
Usta E</span><br />
|
||
<span class="medgenPMjournal">J Clin Ultrasound</span>
|
||
2022 Jul;50(6):795-802.
|
||
Epub 2022 Mar 30
|
||
doi: 10.1002/jcu.23209.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35355279" target="_blank">35355279</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22726404">Visceral heterotaxy in the developing world.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Changlani DK,
|
||
Kotecha M,
|
||
Changlani TD,
|
||
Varghese R,
|
||
Kumar RS</span><br />
|
||
<span class="medgenPMjournal">Heart Lung Circ</span>
|
||
2012 Sep;21(9):598-605.
|
||
Epub 2012 Jun 20
|
||
doi: 10.1016/j.hlc.2012.05.739.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22726404" target="_blank">22726404</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21233261">Experience with bidirectional cavopulmonary anastomosis and modified Fontan operation in patients with single ventricle and concomitant visceral heterotaxy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yurlov IA,
|
||
Podzolkov VP,
|
||
Zelenikin MM,
|
||
Kovalev DV,
|
||
Babaev GK,
|
||
Putiato NA,
|
||
Zaets SB</span><br />
|
||
<span class="medgenPMjournal">Interact Cardiovasc Thorac Surg</span>
|
||
2011 Apr;12(4):563-8.
|
||
Epub 2011 Jan 13
|
||
doi: 10.1510/icvts.2010.253567.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21233261" target="_blank">21233261</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11005603">Omental flap for mediastinitis after median sternotomy in asplenia syndrome and gut malrotation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aeba R,
|
||
Katogi T,
|
||
Moro K,
|
||
Kawada S</span><br />
|
||
<span class="medgenPMjournal">Thorac Cardiovasc Surg</span>
|
||
2000 Aug;48(4):243-4.
|
||
doi: 10.1055/s-2000-6891.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11005603" target="_blank">11005603</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2039676">Prenatal diagnosis of a complex fetal cardiac malformation associated with asplenia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mauser I,
|
||
Deutinger J,
|
||
Bernaschek G</span><br />
|
||
<span class="medgenPMjournal">Br Heart J</span>
|
||
1991 May;65(5):293-5.
|
||
doi: 10.1136/hrt.65.5.293.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2039676" target="_blank">2039676</a><a href="/pmc/articles/PMC1024634" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Visceral%20heterotaxy%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 (20)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29559246">Intrahepatic cholangiocarcinoma after Fontan procedure in an adult with visceral heterotaxy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang D,
|
||
Marshall D,
|
||
Veldtman G,
|
||
Gupta A,
|
||
Trout AT,
|
||
Villafane J,
|
||
Bove K</span><br />
|
||
<span class="medgenPMjournal">Pathol Res Pract</span>
|
||
2018 Jun;214(6):914-918.
|
||
Epub 2018 Mar 15
|
||
doi: 10.1016/j.prp.2018.03.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29559246" target="_blank">29559246</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12031727">Usefulness of cardiac transplantation in children with visceral heterotaxy (asplenic and polysplenic syndromes and single right-sided spleen with levocardia) and comparison of results with cardiac transplantation in children with dilated cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Larsen RL,
|
||
Eguchi JH,
|
||
Mulla NF,
|
||
Johnston JK,
|
||
Fitts J,
|
||
Kuhn MA,
|
||
Razzouk AJ,
|
||
Chinnock RE,
|
||
Bailey LL</span><br />
|
||
<span class="medgenPMjournal">Am J Cardiol</span>
|
||
2002 Jun 1;89(11):1275-9.
|
||
doi: 10.1016/s0002-9149(02)02325-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12031727" target="_blank">12031727</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9464611">Long-term follow-up of surgical patients with single-ventricle physiology: prognostic anatomical determinants.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aeba R,
|
||
Katogi T,
|
||
Takeuchi S,
|
||
Kawada S</span><br />
|
||
<span class="medgenPMjournal">Cardiovasc Surg</span>
|
||
1997 Oct;5(5):526-32.
|
||
doi: 10.1016/s0967-2109(97)00052-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9464611" target="_blank">9464611</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6622295">Asplenia and polysplenia malformation complexes explained by abnormal embryonic body curvature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hutchins GM,
|
||
Moore GW,
|
||
Lipford EH,
|
||
Haupt HM,
|
||
Walker MC</span><br />
|
||
<span class="medgenPMjournal">Pathol Res Pract</span>
|
||
1983 Jun;177(1):60-76.
|
||
doi: 10.1016/S0344-0338(83)80044-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6622295" target="_blank">6622295</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Visceral%20heterotaxy%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 (4)</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 mgSection" id="ID_106">
|
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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=C3178805%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (2)</a></li>
|
||
<li><a href="/gtr/tests?term=C3178805%5bDISCUI%5d&filter=method%3A2%5F17" target="_blank">Mutation scanning of the entire coding region (3)</a></li>
|
||
<li><a href="/gtr/tests?term=C3178805%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (5)</a></li>
|
||
<li><a href="/gtr/tests?term=C3178805%5bDISCUI%5d&filter=method%3A2%5F19" target="_blank">Targeted variant analysis (1)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C3178805%5bDISCUI%5d" target="_blank">See all (8)</a></total></li>
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||
</ul></div>
|
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</div>
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||
|
||
<div class="portlet mgSection" id="ID_119">
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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/phenotypicSeries/PS306955" target="_blank">OMIM</a></li><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=450" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Visceral%20heterotaxy" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
||
<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=(%22visceral%20heterotaxy%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></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Visceral%20heterotaxy" target="_blank">MedlinePlus</a></li><li><a href="https://medlineplus.gov/genetics/condition/heterotaxy-syndrome" target="_blank">MedlinePlusGenetics (GHR)</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/10875/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
|
||
</div>
|
||
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|
||
<div class="portlet brieflink">
|
||
<div class="portlet_head">
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<h3>Reviews</h3>
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||
<ul>
|
||
<li>
|
||
<a href="/pubmed/clinical?term=Visceral%20heterotaxy" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed?term=Visceral%20heterotaxy%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
|
||
</li>
|
||
</ul>
|
||
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|
||
</div>
|
||
|
||
<!-- MedGen supplemental column ends here -->
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||
<div class="portlet brieflink">
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||
<div class="portlet_head">
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||
<div class="portlet_title">
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<h3>Related information</h3>
|
||
</div>
|
||
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<div class="portlet_content DiscoveryDbLinks">
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<ul>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=465273" ref="log$=recordlinks">ClinVar</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related medical variations</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/gtr/tests?term=C3178805[DISCUI]" ref="log$=recordlinks">GTR</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related information in GTR</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/gtr/tests?term=C3178805[DISCUI]&test_type=Clinical" ref="log$=recordlinks">GTR(Clinical)</a>
|
||
<div class="brieflinkpop offscreen_noflow">Clinical tests in GTR</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/mesh?LinkName=medgen_mesh&from_uid=465273" ref="log$=recordlinks">MeSH</a>
|
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<div class="brieflinkpop offscreen_noflow">Related Medical Subject Headings</div>
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</li>
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||
<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=465273" ref="log$=recordlinks">PMC Articles</a>
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<div class="brieflinkpop offscreen_noflow">Related information in PubMed Central Links</div>
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</li>
|
||
<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=465273" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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</li>
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||
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|
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|
||
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||
<div class="portlet">
|
||
<div class="portlet_head">
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<div class="portlet_title">
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<h3>Recent activity</h3>
|
||
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<div class="col-lg-12 centered-lg">
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||
<nav class="bottom-links">
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||
<ul class="mt-3">
|
||
<li>
|
||
<a class="text-white" href="//www.nlm.nih.gov/">NLM</a>
|
||
</li>
|
||
<li>
|
||
<a class="text-white" href="https://www.nih.gov/">NIH</a>
|
||
</li>
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||
<li>
|
||
<a class="text-white" href="https://www.hhs.gov/">HHS</a>
|
||
</li>
|
||
<li>
|
||
<a class="text-white" href="https://www.usa.gov/">USA.gov</a>
|
||
</li>
|
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</ul>
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||
</nav>
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||
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</div>
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</section>
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<script type="text/javascript" src="/portal/portal3rc.fcgi/rlib/js/InstrumentOmnitureBaseJS/InstrumentNCBIConfigJS/InstrumentNCBIBaseJS/InstrumentPageStarterJS.js?v=1"> </script>
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<script type="text/javascript" src="/portal/portal3rc.fcgi/static/js/hfjs2.js"> </script>
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