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<!--
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||
UID=854360
|
||
ConceptID=C3887498
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Bifid ureter</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>854360</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.">C3887498</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Bifid ureters</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:0030037">HP:0030037</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">Incomplete duplication of the ureter. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
||
</div>
|
||
|
||
<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></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">Bifid ureter</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/52948" ref="tree=MeSH" title="MedGen record for Abnormality of the genitourinary system">Abnormality of the genitourinary system</a></span><ul><li><span class="TLline"><a href="/medgen/867444" ref="tree=MeSH" title="MedGen record for Abnormality of the urinary system">Abnormality of the urinary system</a></span><ul><li><span class="TLline"><a href="/medgen/869219" ref="tree=MeSH" title="MedGen record for Abnormality of the upper urinary tract">Abnormality of the upper urinary tract</a></span><ul><li><span class="TLline"><a href="/medgen/374455" ref="tree=MeSH" title="MedGen record for Abnormality of the ureter">Abnormality of the ureter</a></span><ul><li><span class="TLline"><a href="/medgen/1685655" ref="tree=MeSH" title="MedGen record for Abnormal ureter morphology">Abnormal ureter morphology</a></span><ul><li><span class="TLline"><a href="/medgen/66380" ref="tree=MeSH" title="MedGen record for Ureteral duplication">Ureteral duplication</a></span><ul><li><span class="matched_ds">Bifid ureter</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_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_42055"><div><strong>Focal dermal hypoplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>42055</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:">C0016395</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">PORCN-related developmental disorders include a spectrum of highly variable multisystem disorders caused by developmental abnormalities in mesodermal and ectodermal structures primarily involving the skin, limbs, eyes, and face. The manifestations vary among affected individuals, and many have only a subset of the characteristic features. Skin manifestations present at birth include atrophic and hypoplastic areas of skin; cutis aplasia; fat nodules in the dermis manifesting as soft, yellow-pink cutaneous nodules; and pigmentary changes. Verrucous papillomas of the skin and mucous membranes may appear later. The nails can be ridged, dysplastic, or hypoplastic; hair can be sparse or absent. Limb malformations include oligo- and syndactyly and split hand/foot. Developmental abnormalities of the eye can include anophthalmia/microphthalmia, iris and chorioretinal coloboma, and lacrimal duct abnormalities. Craniofacial findings can include facial asymmetry, notched alae nasi, cleft lip and palate, pointed chin, and small, underfolded pinnae. Dental anomalies can include hypodontia, enamel defects, and/or abnormally shaped teeth. Occasional findings include abdominal wall defects, diaphragmatic hernia, and renal anomalies. Psychomotor development is usually normal; some individuals have cognitive impairment and/or behavioral issues.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/42055">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934682"><div><strong>Tall stature-intellectual disability-renal anomalies syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934682</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.">C4310715</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Thauvin-Robinet-Faivre syndrome (TROFAS) is an autosomal recessive disorder characterized by generalized overgrowth, mainly of height, and mildly delayed psychomotor development with mild or severe learning difficulties. More variable features may include congenital heart defects, kidney abnormalities, and skeletal defects. Patients may have an increased risk for Wilms tumor (summary by Akawi et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934682">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1612119"><div><strong>Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1612119</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.">C4539968</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CAKUTHED is an autosomal dominant highly pleiotropic developmental disorder characterized mainly by variable congenital anomalies of the kidney and urinary tract, sometimes resulting in renal dysfunction or failure, dysmorphic facial features, and abnormalities of the outer ear, often with hearing loss. Most patients have global developmental delay (summary by Heidet et al., 2017 and Slavotinek et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1612119">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1642123"><div><strong>Knobloch syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1642123</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.">C4551775</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Knobloch syndrome-1 (KNO1) is an autosomal recessive developmental disorder primarily characterized by typical eye abnormalities, including high myopia, cataracts, dislocated lens, vitreoretinal degeneration, and retinal detachment, with occipital skull defects, which can range from occipital encephalocele to occult cutis aplasia (summary by Aldahmesh et al., 2011). Genetic Heterogeneity of Knobloch Syndrome KNO2 (618458) is caused by mutation in the PAK2 gene (605022) on chromosome 3q29.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1642123">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1612119" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_42055" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Focal dermal hypoplasia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1642123" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Knobloch syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934682" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Tall stature-intellectual disability-renal anomalies syndrome</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/26286110">Congenital malformations of the ureter: anatomical studies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dorko F,
|
||
Tokarčík J,
|
||
Výborná E</span><br />
|
||
<span class="medgenPMjournal">Anat Sci Int</span>
|
||
2016 Jun;91(3):290-4.
|
||
Epub 2015 Aug 19
|
||
doi: 10.1007/s12565-015-0296-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26286110" target="_blank">26286110</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24395870">Chyluria: is retrograde pyelogram mandatory prior to endoscopic sclerotherapy?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Paul S,
|
||
Kumar M,
|
||
Singh V,
|
||
Sankhwar S</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2014 Jan 6;2014
|
||
doi: 10.1136/bcr-2013-200550.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24395870" target="_blank">24395870</a><a href="/pmc/articles/PMC3902324" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21731775">Vesicoureteral reflux and other urinary tract malformations in mice compound heterozygous for Pax2 and Emx2.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Boualia SK,
|
||
Gaitan Y,
|
||
Murawski I,
|
||
Nadon R,
|
||
Gupta IR,
|
||
Bouchard M</span><br />
|
||
<span class="medgenPMjournal">PLoS One</span>
|
||
2011;6(6):e21529.
|
||
Epub 2011 Jun 24
|
||
doi: 10.1371/journal.pone.0021529.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21731775" target="_blank">21731775</a><a href="/pmc/articles/PMC3123351" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1498104">Surgical significance of the duplex kidney with bifid ureter.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Busslinger MI,
|
||
Kaiser G</span><br />
|
||
<span class="medgenPMjournal">Eur J Pediatr Surg</span>
|
||
1992 Jun;2(3):150-1.
|
||
doi: 10.1055/s-2008-1063426.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1498104" target="_blank">1498104</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6679897">Duplication of the renal pelvis and ureter: associated anomalies and pathological conditions.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Inamoto K,
|
||
Tanaka S,
|
||
Takemura K,
|
||
Ikoma F</span><br />
|
||
<span class="medgenPMjournal">Radiat Med</span>
|
||
1983 Jan-Mar;1(1):55-64.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6679897" target="_blank">6679897</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bifid%20ureter%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 (6)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/24395870">Chyluria: is retrograde pyelogram mandatory prior to endoscopic sclerotherapy?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Paul S,
|
||
Kumar M,
|
||
Singh V,
|
||
Sankhwar S</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2014 Jan 6;2014
|
||
doi: 10.1136/bcr-2013-200550.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24395870" target="_blank">24395870</a><a href="/pmc/articles/PMC3902324" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24128825">Ureteral diverticulum: a review of the current literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McLoughlin LC,
|
||
Davis NF,
|
||
Dowling C,
|
||
Eng MP,
|
||
Power RE</span><br />
|
||
<span class="medgenPMjournal">Can J Urol</span>
|
||
2013 Oct;20(5):6893-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24128825" target="_blank">24128825</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10515089">Cephalad renal ectopia, duplication of pelvicalyceal system and patent ductus arteriosus in an adult female.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Al Attia HM</span><br />
|
||
<span class="medgenPMjournal">Scand J Urol Nephrol</span>
|
||
1999 Aug;33(4):257-9.
|
||
doi: 10.1080/003655999750015871.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10515089" target="_blank">10515089</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8987296">Unilateral pulmonary hypoplasia with bifid ureter and pelvis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Prasad R,
|
||
Mukerji PK,
|
||
Kant S,
|
||
Singh AK,
|
||
Narain VS</span><br />
|
||
<span class="medgenPMjournal">Indian J Chest Dis Allied Sci</span>
|
||
1996 Jul-Sep;38(3):205-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8987296" target="_blank">8987296</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1154768">Bifid ureter with blind-ending branch--the radiologist's role in diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harris RD</span><br />
|
||
<span class="medgenPMjournal">West J Med</span>
|
||
1975 Apr;122(4):320-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1154768" target="_blank">1154768</a><a href="/pmc/articles/PMC1129728" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bifid%20ureter%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 (25)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30045270">Obstruction of bifid ureter by two calculi: A case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xiao N,
|
||
Ge B,
|
||
Wang J,
|
||
Zhao H</span><br />
|
||
<span class="medgenPMjournal">Medicine (Baltimore)</span>
|
||
2018 Jul;97(30):e11474.
|
||
doi: 10.1097/MD.0000000000011474.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30045270" target="_blank">30045270</a><a href="/pmc/articles/PMC6078724" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bifid%20ureter%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/24395870">Chyluria: is retrograde pyelogram mandatory prior to endoscopic sclerotherapy?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Paul S,
|
||
Kumar M,
|
||
Singh V,
|
||
Sankhwar S</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2014 Jan 6;2014
|
||
doi: 10.1136/bcr-2013-200550.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24395870" target="_blank">24395870</a><a href="/pmc/articles/PMC3902324" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20306926">Resection of blind ending bifid ureter in a patient with grade V vesicoureteric reflux.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sönmez K,
|
||
Türkyilmaz Z,
|
||
Karabulut R,
|
||
Başaklar AC</span><br />
|
||
<span class="medgenPMjournal">Acta Chir Belg</span>
|
||
2010 Jan-Feb;110(1):109-11.
|
||
doi: 10.1080/00015458.2010.11680581.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20306926" target="_blank">20306926</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1498104">Surgical significance of the duplex kidney with bifid ureter.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Busslinger MI,
|
||
Kaiser G</span><br />
|
||
<span class="medgenPMjournal">Eur J Pediatr Surg</span>
|
||
1992 Jun;2(3):150-1.
|
||
doi: 10.1055/s-2008-1063426.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1498104" target="_blank">1498104</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4020988">Misleading features of blind-ending bifid ureter on computerized tomography examination.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rubenstein DJ,
|
||
Brenner RJ</span><br />
|
||
<span class="medgenPMjournal">J Urol</span>
|
||
1985 Aug;134(2):342-3.
|
||
doi: 10.1016/s0022-5347(17)47158-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4020988" target="_blank">4020988</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bifid%20ureter%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 (4)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33135615">A Rare Case of Ureteral Diverticulum Incidentally Detected During Angiography.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Emekli E,
|
||
Gündoğdu E,
|
||
Özen A,
|
||
Küçükay F</span><br />
|
||
<span class="medgenPMjournal">Curr Med Imaging</span>
|
||
2021;17(4):549-551.
|
||
doi: 10.2174/1573405616999201029123851.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33135615" target="_blank">33135615</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23873247">Bilateral bifid ureter with unilateral renal vasculature variations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chawla K,
|
||
Gupta R,
|
||
Singh HJ,
|
||
Gupta T,
|
||
Aggarwal A,
|
||
Sahni D</span><br />
|
||
<span class="medgenPMjournal">Surg Radiol Anat</span>
|
||
2014 May;36(4):393-6.
|
||
Epub 2013 Jul 20
|
||
doi: 10.1007/s00276-013-1170-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23873247" target="_blank">23873247</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bifid%20ureter%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 (2)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
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|
||
<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 -->
|
||
<div class="rightCol mgCol">
|
||
<div class="portlet mgSection" id="ID_113">
|
||
<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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|
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|
||
<div class="portlet mgSection" id="ID_119">
|
||
<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>
|
||
<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Bifid%20ureter" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_116">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Consumer_resources">Consumer resources</h1><a sid="116" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Bifid%20ureter" target="_blank">MedlinePlus</a></li></ul></div>
|
||
</div>
|
||
</div>
|
||
<div class="portlet brieflink">
|
||
<div class="portlet_head">
|
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<div class="portlet_title">
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<h3>Reviews</h3>
|
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</div>
|
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<div class="portlet_content">
|
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<ul>
|
||
<li>
|
||
<a href="/pubmed/clinical?term=Bifid%20ureter" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed?term=Bifid%20ureter%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
|
||
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|
||
</ul>
|
||
</div>
|
||
</div>
|
||
|
||
<!-- MedGen supplemental column ends here -->
|
||
<div class="portlet brieflink">
|
||
<div class="portlet_head">
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<h3>Related information</h3>
|
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<div class="portlet_content DiscoveryDbLinks">
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<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=854360" ref="log$=recordlinks">PMC Articles</a>
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<div class="brieflinkpop offscreen_noflow">Related information in PubMed Central Links</div>
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|
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<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=854360" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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||
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<h3>Recent activity</h3>
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" cmd="ClearHT" href="?cmd=ClearHT&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory">
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Clear
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d4f90b2f30673f7b61c2db">Bifid ureter</a>
|
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<div class="ralinkpop offscreen_noflow">Bifid ureter<div class="brieflinkpopdesc"></div></div>
|
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<div class="tertiary">MedGen</div>
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<li class="ra_rcd ralinkpopper two_line">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d4f909cde49f3df743ef69">Clitoral hypoplasia</a>
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<div class="ralinkpop offscreen_noflow">Clitoral hypoplasia<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
|
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<li class="ra_rcd ralinkpopper two_line">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d4f9072f30673f7b61ad24">Laryngeal papillomatosis</a>
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<div class="ralinkpop offscreen_noflow">Laryngeal papillomatosis<div class="brieflinkpopdesc"></div></div>
|
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<div class="tertiary">MedGen</div>
|
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=4" href="/portal/utils/pageresolver.fcgi?recordid=67d4f8fd84f3725e59a28b91">PORCN-Related Developmental Disorders - GeneReviews®</a>
|
||
<div class="ralinkpop offscreen_noflow">PORCN-Related Developmental Disorders - GeneReviews®<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary"></div>
|
||
</li>
|
||
<li class="ra_rcd ralinkpopper two_line">
|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=5" href="/portal/utils/pageresolver.fcgi?recordid=67d4f8fccde49f3df743b1e6">Table B. [OMIM Entries for PORCN-Related Developmental Disorders (View All in OM...</a>
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