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<meta name="keywords" content="C0266393, bicervical bicornuate uterus, congenital abnormality, congenital duplication of uterus, didelphic uteri, didelphic uterus, didelphyc uterus, didelphys uterus, double uterus, doubling of uterus, duplex uterus, duplicate uterus, duplicated uterus, duplication of uterus, uterine didelphis, uterine didelphys, uterus didelphis, uterus didelphus, uterus didelphys, uterus duplex, uterus, didelphic, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="A malformation of the uterus in which the uterus is present as a paired organ as a result of the failure of fusion of the mullerian ducts during embryogenesis." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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||
UID=82740
|
||
ConceptID=C0266393
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Uterus didelphys</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>82740</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.">C0266393</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Double uterus</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Congenital duplication of uterus (15545001); Uterus didelphys (15545001); Didelphic uterus (15545001); Uterus didelphus (15545001)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0003762">HP:0003762</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0015834" target="_blank">MONDO:0015834</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=180086">ORPHA180086</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">A malformation of the uterus in which the uterus is present as a paired organ as a result of the failure of fusion of the mullerian ducts during embryogenesis. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
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</div>
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|
||
<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<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 unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Uterus didelphys</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/155422" ref="tree=MeSH" title="MedGen record for Abnormality of the genital system">Abnormality of the genital system</a></span><ul><li><span class="TLline"><a href="/medgen/866746" ref="tree=MeSH" title="MedGen record for Abnormal reproductive system morphology">Abnormal reproductive system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/869393" ref="tree=MeSH" title="MedGen record for Abnormality of the female genitalia">Abnormality of the female genitalia</a></span><ul><li><span class="TLline"><a href="/medgen/871402" ref="tree=MeSH" title="MedGen record for Abnormal morphology of female internal genitalia">Abnormal morphology of female internal genitalia</a></span><ul><li><span class="TLline"><a href="/medgen/78598" ref="tree=MeSH" title="MedGen record for Congenital uterine anomaly">Congenital uterine anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/1371444" ref="tree=MeSH" title="MedGen record for Abnormal uterus morphology">Abnormal uterus morphology</a></span><ul><li><span class="matched_ds">Uterus didelphys</span><ul><li><span class="TLline"><a href="/medgen/1842173" ref="tree=MeSH" title="MedGen record for Bicervical bicornuate uterus and blind hemivagina">Bicervical bicornuate uterus and blind hemivagina</a></span></li><li><span class="TLline"><a href="/medgen/1842271" ref="tree=MeSH" title="MedGen record for Bicervical bicornuate uterus with patent cervix and vagina">Bicervical bicornuate uterus with patent cervix and vagina</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=18090&search=Disease_Classif_Simple&new=1" class="ital bold">this link</a> to review classifications for <span class="ital">Uterus didelphys</span> in Orphanet.</div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_181980"><div><strong>Drash syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>181980</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.">C0950121</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">WT1 disorder is characterized by congenital/infantile or childhood onset of steroid-resistant nephrotic syndrome (SRNS), a progressive glomerulopathy that does not respond to standard steroid therapy. Additional common findings can include disorders of testicular development (with or without abnormalities of the external genitalia and/or müllerian structures) and Wilms tumor. Less common findings are congenital anomalies of the kidney and urinary tract (CAKUT) and gonadoblastoma. While various combinations of renal and other findings associated with a WT1 pathogenic variant were designated as certain syndromes in the past, those designations are now recognized to be part of a phenotypic continuum and are no longer clinically helpful.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/181980">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_374443"><div><strong>Hypoparathyroidism, deafness, renal disease syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>374443</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.">C1840333</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">HDR syndrome (HDRS), also known as Barakat syndrome, is a heterogeneous disorder characterized by the triad of Hypoparathyroidism (H), nerve Deafness (D) and/or Renal disease (R). Variable clinical features include hypogonadotrophic hypogonadism, polycystic ovaries, congenital heart disease, retinitis pigmentosa, and cognitive disability (Barakat et al., 2018).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/374443">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_327078"><div><strong>Mullerian duct anomalies-limb anomalies syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>327078</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.">C1840335</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Mullerian duct anomalies-limb anomalies syndrome is characterised by the association of mullerian duct and distal limb anomalies. It has been described in five individuals from one family. Females presented with anomalies ranging from a vaginal septum to complete duplication of uterus and vagina, and males presented with micropenis. The limb anomalies varied from postaxial polydactyly to severe upper limb hypoplasia with split hand. The mode of transmission is autosomal dominant.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/327078">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_331103"><div><strong>Hand-foot-genital syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>331103</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:">C1841679</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hand-foot-genital syndrome (HFGS) is characterized by limb malformations and urogenital defects. Mild-to-severe bilateral shortening of the thumbs and great toes, caused primarily by shortening of the distal phalanx and/or the first metacarpal or metatarsal, is the most common limb malformation and results in impaired dexterity or apposition of the thumbs. Urogenital malformations include abnormalities of the ureters and urethra and various degrees of incomplete müllerian fusion in females, and hypospadias of variable severity with or without chordee in males. Vesicoureteral reflux, recurrent urinary tract infections, and chronic pyelonephritis may occur; fertility is normal.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/331103">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_335822"><div><strong>Caudal duplication</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>335822</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.">C1842884</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Caudal duplication (CD) is a rare developmental anomaly in which structures derived from the embryonic cloaca and notochord are duplicated to varying extents.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/335822">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_395425"><div><strong>Acro-renal-mandibular syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>395425</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.">C1860166</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A very rare multiple congenital anomalies syndrome with characteristics of limb deficiencies and renal anomalies that include split hand-split foot malformation, renal agenesis, polycystic kidneys, uterine anomalies and severe mandibular hypoplasia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/395425">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_413823"><div><strong>Autosomal dominant omodysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>413823</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.">C2750355</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Omodysplasia-2 (OMOD2) is a rare autosomal dominant skeletal dysplasia characterized by shortened humeri, dislocated radial heads, shortened first metacarpals, craniofacial dysmorphism, and variable genitourinary anomalies (Saal et al., 2015). For a discussion of genetic heterogeneity of OMOD, see 258315.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/413823">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1634931"><div><strong>Short-rib thoracic dysplasia 20 with polydactyly</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1634931</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.">C4693616</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Short-rib thoracic dysplasia (SRTD) with or without polydactyly refers to a group of autosomal recessive skeletal ciliopathies that are characterized by a constricted thoracic cage, short ribs, shortened tubular bones, and a 'trident' appearance of the acetabular roof. SRTD encompasses Ellis-van Creveld syndrome (EVC) and the disorders previously designated as Jeune syndrome or asphyxiating thoracic dystrophy (ATD), short rib-polydactyly syndrome (SRPS), and Mainzer-Saldino syndrome (MZSDS). Polydactyly is variably present, and there is phenotypic overlap in the various forms of SRTDs, which differ by visceral malformation and metaphyseal appearance. Nonskeletal involvement can include cleft lip/palate as well as anomalies of major organs such as the brain, eye, heart, kidneys, liver, pancreas, intestines, and genitalia. Some forms of SRTD are lethal in the neonatal period due to respiratory insufficiency secondary to a severely restricted thoracic cage, whereas others are compatible with life (summary by Huber and Cormier-Daire, 2012 and Schmidts et al., 2013). There is phenotypic overlap with the cranioectodermal dysplasias (Sensenbrenner syndrome; see CED1, 218330).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1634931">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1720440"><div><strong>Genitourinary and/or brain malformation syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1720440</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.">C5394158</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Individuals with PPP1R12A-related urogenital and/or brain malformation syndrome (UBMS) usually present with multiple congenital anomalies, most commonly involving the brain and/or urogenital systems. The brain abnormalities are variable, with the most severe belonging to the holoprosencephaly spectrum and associated with moderate-to-profound intellectual disability, seizures, and feeding difficulties. In individuals without brain involvement, variable degrees of developmental delay and/or intellectual disability may be present, although normal intelligence has been seen in a minority of affected individuals. Eye (strabismus, microphthalmia/anophthalmia) and skeletal abnormalities (kyphoscoliosis, joint contractures) can also be present in affected individuals of either sex. Regardless of the presence of a brain malformation, affected individuals with a 46,XY chromosome complement may have a difference of sex development (DSD) with gonadal dysgenesis associated with ambiguous genitalia or phenotypic female genitalia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1720440">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_395425" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acro-renal-mandibular syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_413823" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant omodysplasia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_335822" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Caudal duplication</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_181980" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Drash syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1720440" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Genitourinary and/or brain malformation syndrome</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (9)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_331103" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hand-foot-genital syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_374443" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypoparathyroidism, deafness, renal disease syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_327078" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mullerian duct anomalies-limb anomalies syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1634931" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Short-rib thoracic dysplasia 20 with polydactyly</a></div></span></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/33873082">Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA): Early diagnosis, treatment and outcomes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yang M,
|
||
Wen S,
|
||
Liu X,
|
||
He D,
|
||
Wei G,
|
||
Wu S,
|
||
Huang Y,
|
||
Ni Y,
|
||
Shi Y,
|
||
Hua Y</span><br />
|
||
<span class="medgenPMjournal">Eur J Obstet Gynecol Reprod Biol</span>
|
||
2021 Jun;261:12-16.
|
||
Epub 2021 Apr 16
|
||
doi: 10.1016/j.ejogrb.2021.03.018.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33873082" target="_blank">33873082</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32127135">Diagnosis and treatment of müllerian malformations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Passos IMPE,
|
||
Britto RL</span><br />
|
||
<span class="medgenPMjournal">Taiwan J Obstet Gynecol</span>
|
||
2020 Mar;59(2):183-188.
|
||
doi: 10.1016/j.tjog.2020.01.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32127135" target="_blank">32127135</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11284660">Clinical implications of uterine malformations and hysteroscopic treatment results.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Grimbizis GF,
|
||
Camus M,
|
||
Tarlatzis BC,
|
||
Bontis JN,
|
||
Devroey P</span><br />
|
||
<span class="medgenPMjournal">Hum Reprod Update</span>
|
||
2001 Mar-Apr;7(2):161-74.
|
||
doi: 10.1093/humupd/7.2.161.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11284660" target="_blank">11284660</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22uterus%20didelphys%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 (9)</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/39227392">Assisted reproductive technology outcomes in women with congenital uterine anomalies: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fedele F,
|
||
Bulfoni A,
|
||
Parazzini F,
|
||
Levi-Setti PE,
|
||
Busnelli A</span><br />
|
||
<span class="medgenPMjournal">Arch Gynecol Obstet</span>
|
||
2024 Nov;310(5):2315-2332.
|
||
Epub 2024 Sep 4
|
||
doi: 10.1007/s00404-024-07666-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39227392" target="_blank">39227392</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36078286">The Impact of Uterus Didelphys on Fertility and Pregnancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ćwiertnia A,
|
||
Borzyszkowska D,
|
||
Golara A,
|
||
Tuczyńska N,
|
||
Kozłowski M,
|
||
Kwiatkowski S,
|
||
Cymbaluk-Płoska A</span><br />
|
||
<span class="medgenPMjournal">Int J Environ Res Public Health</span>
|
||
2022 Aug 25;19(17)
|
||
doi: 10.3390/ijerph191710571.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36078286" target="_blank">36078286</a><a href="/pmc/articles/PMC9518538" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30377758">Early vaginal replacement in cloacal malformation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sharma S,
|
||
Gupta DK</span><br />
|
||
<span class="medgenPMjournal">Pediatr Surg Int</span>
|
||
2019 Feb;35(2):263-269.
|
||
Epub 2018 Oct 30
|
||
doi: 10.1007/s00383-018-4407-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30377758" target="_blank">30377758</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22470758">Uterus didelphys with unilateral distal vaginal agenesis and ipsilateral renal agenesis: common presentation of an unusual variation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adair L 2nd,
|
||
Georgiades M,
|
||
Osborne R,
|
||
Ng T</span><br />
|
||
<span class="medgenPMjournal">J Radiol Case Rep</span>
|
||
2011;5(1):1-8.
|
||
Epub 2011 Jan 1
|
||
doi: 10.3941/jrcr.v5i1.572.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22470758" target="_blank">22470758</a><a href="/pmc/articles/PMC3303417" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3618142">Uterus didelphys associated with bilateral dermoid cysts and polycystic ovarian disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sørensen SS,
|
||
Balslev E</span><br />
|
||
<span class="medgenPMjournal">Acta Obstet Gynecol Scand</span>
|
||
1987;66(2):171-3.
|
||
doi: 10.3109/00016348709083042.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3618142" target="_blank">3618142</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uterus%20didelphys%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 (52)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36150723">Young adolescent with trisomy 13.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kramer BCE,
|
||
Abdullahi NS,
|
||
Ten Have LC,
|
||
van den Elzen APM</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2022 Sep 23;15(9)
|
||
doi: 10.1136/bcr-2021-246514.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36150723" target="_blank">36150723</a><a href="/pmc/articles/PMC9511538" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33236794">New Consideration of Herlyn-Werner-Wunderlich Syndrome Diagnosed by Ultrasound.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu M,
|
||
Zhang L,
|
||
Xia Y,
|
||
Huang X,
|
||
Ye T,
|
||
Zhang Y,
|
||
Qi Z,
|
||
Wang L,
|
||
Lai X,
|
||
Dai Q,
|
||
Jiang Y</span><br />
|
||
<span class="medgenPMjournal">J Ultrasound Med</span>
|
||
2021 Sep;40(9):1893-1900.
|
||
Epub 2020 Nov 25
|
||
doi: 10.1002/jum.15572.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33236794" target="_blank">33236794</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32127135">Diagnosis and treatment of müllerian malformations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Passos IMPE,
|
||
Britto RL</span><br />
|
||
<span class="medgenPMjournal">Taiwan J Obstet Gynecol</span>
|
||
2020 Mar;59(2):183-188.
|
||
doi: 10.1016/j.tjog.2020.01.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32127135" target="_blank">32127135</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30597168">Herlyn-Werner-Wunderlich Syndrome: Report of a Prenatally Recognised Case and Review of the Literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tuna T,
|
||
Estevão-Costa J,
|
||
Ramalho C,
|
||
Fragoso AC</span><br />
|
||
<span class="medgenPMjournal">Urology</span>
|
||
2019 Mar;125:205-209.
|
||
Epub 2018 Dec 28
|
||
doi: 10.1016/j.urology.2018.12.022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30597168" target="_blank">30597168</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9526822">Uterus didelphys with unilateral imperforate hemivagina and ipsilateral renal agenesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Altintaş A</span><br />
|
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<div class="nl"><a target="_blank" href="/pubmed/36823415">Anatomical variations, treatment and outcomes of Herlyn-Werner-Wunderlich syndrome: a literature review of 1673 cases.</a></div>
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Wang J,
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<div class="portlet_content ln"><span class="medgenPMauthor">Tyagi A,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uterus%20didelphys%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 (14)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/39227392">Assisted reproductive technology outcomes in women with congenital uterine anomalies: a systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Fedele F,
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Bulfoni A,
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Parazzini F,
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<span class="bold">PMID: </span><a href="/pubmed/39227392" target="_blank">39227392</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28118070">Endometrial cancer with congenital uterine anomalies: 3 case reports and a literature review.</a></div>
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Zhang J,
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Tian W,
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<div class="nl"><a target="_blank" href="/pubmed/25591566">New classification of Herlyn-Werner-Wunderlich syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Zhu L,
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Chen N,
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Tong JL,
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<div class="nl"><a target="_blank" href="/pubmed/9526822">Uterus didelphys with unilateral imperforate hemivagina and ipsilateral renal agenesis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Altintaş A</span><br />
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1998 Feb;11(1):25-7.
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<span class="bold">PMID: </span><a href="/pubmed/9526822" target="_blank">9526822</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/1555685">Uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis: the University of Minnesota experience.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Stassart JP,
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Nagel TC,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uterus%20didelphys%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 (31)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/35953315">A case of didelphys uterus: tackling the double trouble adenomyosis and infertility.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Bindra V,
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Reddy CA,
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Swetha P,
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Madhavi N</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/35953315" target="_blank">35953315</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/22160342">Plicae palmatae of the cervical canals in uterus didelphys: MR imaging.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Takahata A,
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<div class="nl"><a target="_blank" href="/pubmed/17430731">Asymmetric lateral distribution of obstructed hemivagina and renal agenesis in women with uterus didelphys: institutional case series and a systematic literature review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Vercellini P,
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Daguati R,
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Somigliana E,
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Viganò P,
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Lanzani A,
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<div class="portlet_content ln"><span class="medgenPMauthor">Evans JA,
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<div class="nl"><a target="_blank" href="/pubmed/1563657">Uterus didelphys and pregnancy: an unusual case in an 18-year-old patient.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Karpathios SE,
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Phylactou M,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uterus%20didelphys%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 (22)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/39227392">Assisted reproductive technology outcomes in women with congenital uterine anomalies: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fedele F,
|
||
Bulfoni A,
|
||
Parazzini F,
|
||
Levi-Setti PE,
|
||
Busnelli A</span><br />
|
||
<span class="medgenPMjournal">Arch Gynecol Obstet</span>
|
||
2024 Nov;310(5):2315-2332.
|
||
Epub 2024 Sep 4
|
||
doi: 10.1007/s00404-024-07666-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39227392" target="_blank">39227392</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36823415">Anatomical variations, treatment and outcomes of Herlyn-Werner-Wunderlich syndrome: a literature review of 1673 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu Y,
|
||
Li Z,
|
||
Dou Y,
|
||
Wang J,
|
||
Li Y</span><br />
|
||
<span class="medgenPMjournal">Arch Gynecol Obstet</span>
|
||
2023 Nov;308(5):1409-1417.
|
||
Epub 2023 Feb 24
|
||
doi: 10.1007/s00404-022-06856-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36823415" target="_blank">36823415</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34274235">Multiple variants of obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome - one clinical center case series and the systematic review of 734 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kudela G,
|
||
Wiernik A,
|
||
Drosdzol-Cop A,
|
||
Machnikowska-Sokołowska M,
|
||
Gawlik A,
|
||
Hyla-Klekot L,
|
||
Gruszczyńska K,
|
||
Koszutski T</span><br />
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<span class="medgenPMjournal">J Pediatr Urol</span>
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||
2021 Oct;17(5):653.e1-653.e9.
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||
Epub 2021 Jun 30
|
||
doi: 10.1016/j.jpurol.2021.06.023.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34274235" target="_blank">34274235</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17430731">Asymmetric lateral distribution of obstructed hemivagina and renal agenesis in women with uterus didelphys: institutional case series and a systematic literature review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vercellini P,
|
||
Daguati R,
|
||
Somigliana E,
|
||
Viganò P,
|
||
Lanzani A,
|
||
Fedele L</span><br />
|
||
<span class="medgenPMjournal">Fertil Steril</span>
|
||
2007 Apr;87(4):719-24.
|
||
doi: 10.1016/j.fertnstert.2007.01.173.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17430731" target="_blank">17430731</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uterus%20didelphys%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
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|
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<div class="supplemental col three_col last">
|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=180086" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Uterus%20didelphys" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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