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<meta name="keywords" content="C1835796, congenital abnormality, cross-fused renal ectopia, crossed fused renal ectopia, crossed-fused renal ectopia, ectopic kidney with fusion, finding, 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 developmental anomaly in which the kidneys are fused and localized on the same side of the midline. This anomaly is thought to result from disruption of the normal embryologic migration of the kidneys." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=372130
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ConceptID=C1835796
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Crossed fused renal ectopia</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>372130</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.">C1835796</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Cross-fused renal ectopia; Ectopic kidney with fusion</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0004736">HP:0004736</a></td></tr>
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</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_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln">A developmental anomaly in which the kidneys are fused and localized on the same side of the midline. This anomaly is thought to result from disruption of the normal embryologic migration of the kidneys. [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_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="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">Crossed fused renal ectopia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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/78593" ref="tree=MeSH" title="MedGen record for Abnormality of the kidney">Abnormality of the kidney</a></span><ul><li><span class="TLline"><a href="/medgen/1633142" ref="tree=MeSH" title="MedGen record for Abnormal renal morphology">Abnormal renal morphology</a></span><ul><li><span class="TLline"><a href="/medgen/866621" ref="tree=MeSH" title="MedGen record for Abnormal localization of kidney">Abnormal localization of kidney</a></span><ul><li><span class="TLline"><a href="/medgen/68661" ref="tree=MeSH" title="MedGen record for Ectopic kidney">Ectopic kidney</a></span><ul><li><span class="matched_ds">Crossed fused renal ectopia</span><ul><li><span class="TLline"><a href="/medgen/1814383" ref="tree=MeSH" title="MedGen record for Disc kidney">Disc kidney</a></span></li><li><span class="TLline"><a href="/medgen/1814380" ref="tree=MeSH" title="MedGen record for Inferior crossed fused renal ectopia">Inferior crossed fused renal ectopia</a></span></li><li><span class="TLline"><a href="/medgen/1813216" ref="tree=MeSH" title="MedGen record for L-shaped kidney">L-shaped kidney</a></span></li><li><span class="TLline"><a href="/medgen/1814381" ref="tree=MeSH" title="MedGen record for Sigmoid kidney">Sigmoid kidney</a></span></li><li><span class="TLline"><a href="/medgen/1814384" ref="tree=MeSH" title="MedGen record for Superior crossed-fused renal ectopia">Superior crossed-fused renal ectopia</a></span></li><li><span class="TLline"><a href="/medgen/1814382" ref="tree=MeSH" title="MedGen record for Unilateral lump kidney">Unilateral lump kidney</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
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|
||
<div class="portlet mgSection" id="ID_112">
|
||
<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_162897"><div><strong>Kabuki syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>162897</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.">C0796004</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Kabuki syndrome (KS) is characterized by typical facial features (long palpebral fissures with eversion of the lateral third of the lower eyelid; arched and broad eyebrows; short columella with depressed nasal tip; large, prominent, or cupped ears), minor skeletal anomalies, persistence of fetal fingertip pads, mild-to-moderate intellectual disability, and postnatal growth deficiency. Other findings may include: congenital heart defects, genitourinary anomalies, cleft lip and/or palate, gastrointestinal anomalies including anal atresia, ptosis and strabismus, and widely spaced teeth and hypodontia. Functional differences can include: increased susceptibility to infections and autoimmune disorders, seizures, endocrinologic abnormalities (including isolated premature thelarche in females), feeding problems, and hearing loss.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/162897">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_301647"><div><strong>Duane-radial ray syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>301647</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.">C1623209</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">SALL4-related disorders include Duane-radial ray syndrome (DRRS, Okihiro syndrome), acro-renal-ocular syndrome (AROS), and SALL4-related Holt-Oram syndrome (HOS) – three phenotypes previously thought to be distinct entities. DRRS is characterized by uni- or bilateral Duane anomaly and radial ray malformation that can include thenar hypoplasia and/or hypoplasia or aplasia of the thumbs, hypoplasia or aplasia of the radii, shortening and radial deviation of the forearms, triphalangeal thumbs, and duplication of the thumb (preaxial polydactyly). AROS is characterized by radial ray malformations, renal abnormalities (mild malrotation, ectopia, horseshoe kidney, renal hypoplasia, vesicoureteral reflux, bladder diverticula), ocular coloboma, and Duane anomaly. Rarely, pathogenic variants in SALL4 may cause clinically typical HOS (i.e., radial ray malformations and cardiac malformations without additional features).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/301647">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_358131"><div><strong>Orofaciodigital syndrome V</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>358131</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.">C1868118</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Orofaciodigital syndrome V (OFD5) is an autosomal recessive disorder characterized by cleft palate/uvula, lobulated tongue, frontal bossing, hypertelorism, postaxial polydactyly, and impaired intellectual development (summary by Faily et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/358131">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_394424"><div><strong>Syndactyly-telecanthus-anogenital and renal malformations syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>394424</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.">C2678045</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Syndrome with the association of toe syndactyly, facial dysmorphism including telecanthus and a broad nasal tip, urogenital malformations and anal atresia. Around ten cases have been reported so far. The syndrome is caused by mutations in the FAM58A gene (located on the X chromosome) encoding a protein of unknown function.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/394424">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_905986"><div><strong>MEND syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>905986</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.">C4085243</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Male EBP disorder with neurologic defects (MEND) is an X-linked recessive disorder representing a continuous phenotypic spectrum with variable manifestations associated with a defect in sterol biosynthesis. Features include intellectual disability, short stature, scoliosis, digital abnormalities, cataracts, and dermatologic abnormalities. Not all patients show all features, and the severity is highly variable. Molecular studies indicate that affected males are hemizygous for a nonmosaic hypomorphic EBP allele. Carrier females are generally clinically asymptomatic, but may show biochemical abnormalities (summary by Arnold et al., 2012 and Barboza-Cerda et al., 2014).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/905986">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1381939"><div><strong>Townes-Brocks syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1381939</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.">C4479534</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1381939">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1375936"><div><strong>Stankiewicz-Isidor syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1375936</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.">C4479599</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Stankiewicz-Isidor syndrome (STISS) is a neurodevelopmental disorder characterized by delayed psychomotor development, intellectual disability, behavioral disorders, mild craniofacial anomalies, and variable congenital defects of the cardiac and/or urogenital systems (summary by Kury et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1375936">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1648412"><div><strong>Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1648412</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.">C4748348</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">MFRG is an autosomal recessive syndrome in which microcephaly, unilateral renal agenesis, ambiguous genitalia, and facial dysmorphisms, including severe micrognathia, are observed in most patients. Variable brain, cardiac, and skeletal anomalies are present, including corpus callosum agenesis or dysgenesis, lissencephaly, atrial and ventricular septal defects, patent ductus arteriosus, hypoplastic right ventricle, and joint contractures (Shaheen et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1648412">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1803276"><div><strong>Chilton-Okur-Chung neurodevelopmental syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1803276</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.">C5677022</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Chilton-Okur-Chung neurodevelopmental syndrome (CHOCNS) is characterized mainly by global developmental delay with variably impaired intellectual development and occasional speech delay. Most patients have behavioral abnormalities, including autism spectrum disorder, ADHD, and aggression. About half of patients have dysmorphic facial features, and about half have nonspecific brain abnormalities, including thin corpus callosum. Rare involvement of other organ systems may be present. At least 1 child with normal development at age 2.5 years has been reported (Chilton et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1803276">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1803276" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chilton-Okur-Chung neurodevelopmental syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_301647" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Duane-radial ray syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_162897" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Kabuki syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_905986" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">MEND syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1648412" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia 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_358131" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Orofaciodigital syndrome V</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1375936" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Stankiewicz-Isidor syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_394424" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Syndactyly-telecanthus-anogenital and renal malformations syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1381939" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Townes-Brocks syndrome 2</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/21084958">Prenatal diagnosis of renal developmental anomalies associated with an empty renal fossa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Oh KY,
|
||
Holznagel DE,
|
||
Ameli JR,
|
||
Sohaey R</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Q</span>
|
||
2010 Dec;26(4):233-40.
|
||
doi: 10.1097/RUQ.0b013e3181f573fd.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21084958" target="_blank">21084958</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22crossed%20fused%20renal%20ectopia%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 (1)</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/34090309">Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Su J,
|
||
Qin Z,
|
||
Fu H,
|
||
Luo J,
|
||
Huang Y,
|
||
Huang P,
|
||
Zhang S,
|
||
Liu T,
|
||
Lu W,
|
||
Li W,
|
||
Jiang T,
|
||
Wei S,
|
||
Yang S,
|
||
Shen Y</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
|
||
2022 Feb;59(2):226-233.
|
||
doi: 10.1002/uog.23702.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34090309" target="_blank">34090309</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33004190">Crossed fused renal ectopia: Diagnosis and prognosis as a single-center experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sarhan O,
|
||
El Helaly A,
|
||
Al Otay A,
|
||
Al Bedaiwi K,
|
||
Al Ghanbar M,
|
||
Nakshabandi Z</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Surg</span>
|
||
2021 Sep;56(9):1632-1637.
|
||
Epub 2020 Sep 8
|
||
doi: 10.1016/j.jpedsurg.2020.08.030.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33004190" target="_blank">33004190</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30608912">Dual-Tracer PET/CT Differentiates 2 Types of Primary Cancers and Metastases in a Patient With Crossed Fused Renal Ectopia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ho CL,
|
||
Chen S,
|
||
Leung YL,
|
||
Cheng KC,
|
||
Wong YH</span><br />
|
||
<span class="medgenPMjournal">Clin Nucl Med</span>
|
||
2019 Feb;44(2):157-158.
|
||
doi: 10.1097/RLU.0000000000002390.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30608912" target="_blank">30608912</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29900826">Urothelial metaplasia of the seminal vesicle and ejaculatory duct associated with crossed-fused renal ectopia and Hutch diverticulum of the bladder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chezar K,
|
||
Gotto G,
|
||
Medlicott S,
|
||
Trpkov K</span><br />
|
||
<span class="medgenPMjournal">Can J Urol</span>
|
||
2018 Jun;25(3):9360-9362.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29900826" target="_blank">29900826</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27303239">Endovascular Abdominal Aortic Aneurysm Repair by Means of the Chimney Technique in a Patient with Crossed Fused Renal Ectopia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kfoury E,
|
||
Almanfi A,
|
||
Dougherty KG,
|
||
Krajcer Z</span><br />
|
||
<span class="medgenPMjournal">Tex Heart Inst J</span>
|
||
2016 Jun;43(3):232-5.
|
||
Epub 2016 Jun 1
|
||
doi: 10.14503/THIJ-15-5025.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27303239" target="_blank">27303239</a><a href="/pmc/articles/PMC4894702" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Crossed%20fused%20renal%20ectopia%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 (13)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33004190">Crossed fused renal ectopia: Diagnosis and prognosis as a single-center experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sarhan O,
|
||
El Helaly A,
|
||
Al Otay A,
|
||
Al Bedaiwi K,
|
||
Al Ghanbar M,
|
||
Nakshabandi Z</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Surg</span>
|
||
2021 Sep;56(9):1632-1637.
|
||
Epub 2020 Sep 8
|
||
doi: 10.1016/j.jpedsurg.2020.08.030.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33004190" target="_blank">33004190</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31331806">Crossed fused renal ectopia in children: a review of clinical profile, surgical challenges, and outcome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Loganathan AK,
|
||
Bal HS</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Urol</span>
|
||
2019 Aug;15(4):315-321.
|
||
Epub 2019 Jun 26
|
||
doi: 10.1016/j.jpurol.2019.06.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31331806" target="_blank">31331806</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26945665">Bladder Agenesis Associated with Crossed Fused Renal Ectopia and Vertebral Anomalies: A Rare Entity.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sailo SL,
|
||
Sailo L</span><br />
|
||
<span class="medgenPMjournal">Urol J</span>
|
||
2016 Mar 5;13(1):2579-80.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26945665" target="_blank">26945665</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26823352">Crossed fused renal ectopia with chyluria: a rare presentation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh K,
|
||
Kumar M,
|
||
Jhanwar A,
|
||
Sankhwar S</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2016 Jan 28;2016
|
||
doi: 10.1136/bcr-2015-213050.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26823352" target="_blank">26823352</a><a href="/pmc/articles/PMC4735158" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25241837">Crossed renal ectopia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pelegrí Gabarró J,
|
||
Guiote Partido I,
|
||
Oliva Encina J,
|
||
Rioja Sanz C</span><br />
|
||
<span class="medgenPMjournal">Arch Esp Urol</span>
|
||
2014 Sep;67(7):634-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25241837" target="_blank">25241837</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Crossed%20fused%20renal%20ectopia%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 (48)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36958616">Crossed fused renal ectopia during paraaortic lymphadenectomy for cervical cancer.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tsaousidis G,
|
||
Zitzelsberger U,
|
||
Papathemelis T</span><br />
|
||
<span class="medgenPMjournal">J Minim Invasive Gynecol</span>
|
||
2023 Jul;30(7):525-526.
|
||
Epub 2023 Mar 21
|
||
doi: 10.1016/j.jmig.2023.03.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36958616" target="_blank">36958616</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26823352">Crossed fused renal ectopia with chyluria: a rare presentation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh K,
|
||
Kumar M,
|
||
Jhanwar A,
|
||
Sankhwar S</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2016 Jan 28;2016
|
||
doi: 10.1136/bcr-2015-213050.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26823352" target="_blank">26823352</a><a href="/pmc/articles/PMC4735158" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21831590">A novel approach to the management of an inflammatory abdominal aortic aneurysm associated with crossed-fused renal ectopia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tadros RO,
|
||
Malik RK,
|
||
Ellozy SH,
|
||
Marin ML,
|
||
Faries PL,
|
||
Vouyouka AG</span><br />
|
||
<span class="medgenPMjournal">Ann Vasc Surg</span>
|
||
2011 Oct;25(7):984.e9-14.
|
||
Epub 2011 Aug 10
|
||
doi: 10.1016/j.avsg.2011.05.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21831590" target="_blank">21831590</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11555015">Resection of an L-shaped kidney with renal cell carcinoma using a microwave tissue coagulator.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tsunoe H,
|
||
Yasumasu T,
|
||
Tanaka M,
|
||
Kai N,
|
||
Naito S</span><br />
|
||
<span class="medgenPMjournal">Int J Urol</span>
|
||
2001 Aug;8(8):459-62.
|
||
doi: 10.1046/j.1442-2042.2001.00348.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11555015" target="_blank">11555015</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10461116">Vesicocolonic fistula four years after augmentation colocystoplasty.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gofrit ON,
|
||
Pode D,
|
||
Landau EH</span><br />
|
||
<span class="medgenPMjournal">Urol Int</span>
|
||
1999;62(2):117-8.
|
||
doi: 10.1159/000030371.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10461116" target="_blank">10461116</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Crossed%20fused%20renal%20ectopia%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 (6)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33004190">Crossed fused renal ectopia: Diagnosis and prognosis as a single-center experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sarhan O,
|
||
El Helaly A,
|
||
Al Otay A,
|
||
Al Bedaiwi K,
|
||
Al Ghanbar M,
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Nakshabandi Z</span><br />
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<span class="medgenPMjournal">J Pediatr Surg</span>
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2021 Sep;56(9):1632-1637.
|
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Epub 2020 Sep 8
|
||
doi: 10.1016/j.jpedsurg.2020.08.030.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33004190" target="_blank">33004190</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31331806">Crossed fused renal ectopia in children: a review of clinical profile, surgical challenges, and outcome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Loganathan AK,
|
||
Bal HS</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Urol</span>
|
||
2019 Aug;15(4):315-321.
|
||
Epub 2019 Jun 26
|
||
doi: 10.1016/j.jpurol.2019.06.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31331806" target="_blank">31331806</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29900826">Urothelial metaplasia of the seminal vesicle and ejaculatory duct associated with crossed-fused renal ectopia and Hutch diverticulum of the bladder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chezar K,
|
||
Gotto G,
|
||
Medlicott S,
|
||
Trpkov K</span><br />
|
||
<span class="medgenPMjournal">Can J Urol</span>
|
||
2018 Jun;25(3):9360-9362.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29900826" target="_blank">29900826</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22056611">L-shaped right-to-left crossed-fused renal ectopia with left dysplastic ureter.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Song W,
|
||
Yang J,
|
||
Zhu L,
|
||
Liu L</span><br />
|
||
<span class="medgenPMjournal">Urol Int</span>
|
||
2012;88(2):241-4.
|
||
Epub 2011 Nov 1
|
||
doi: 10.1159/000332428.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22056611" target="_blank">22056611</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15539878">Sonographic findings of fetuses with an empty renal fossa and normal amniotic fluid volume.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yuksel A,
|
||
Batukan C</span><br />
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||
<span class="medgenPMjournal">Fetal Diagn Ther</span>
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||
2004 Nov-Dec;19(6):525-32.
|
||
doi: 10.1159/000080166.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15539878" target="_blank">15539878</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Crossed%20fused%20renal%20ectopia%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 (9)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33069370">Mayer-Rokitansky-Küster-Hauser syndrome with rare findings of inferior crossed-fused renal ectopia and Gartner's duct cyst: a video case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liang G,
|
||
Xia W,
|
||
Liang Y,
|
||
Zhu Q,
|
||
Zou L,
|
||
Zhang J,
|
||
Jiang H</span><br />
|
||
<span class="medgenPMjournal">Fertil Steril</span>
|
||
2021 Feb;115(2):525-527.
|
||
Epub 2020 Oct 14
|
||
doi: 10.1016/j.fertnstert.2020.08.1433.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33069370" target="_blank">33069370</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32737436">Rare heterozygous GDF6 variants in patients with renal anomalies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Martens H,
|
||
Hennies I,
|
||
Getwan M,
|
||
Christians A,
|
||
Weiss AC,
|
||
Brand F,
|
||
Gjerstad AC,
|
||
Christians A,
|
||
Gucev Z,
|
||
Geffers R,
|
||
Seeman T,
|
||
Kispert A,
|
||
Tasic V,
|
||
Bjerre A,
|
||
Lienkamp SS,
|
||
Haffner D,
|
||
Weber RG</span><br />
|
||
<span class="medgenPMjournal">Eur J Hum Genet</span>
|
||
2020 Dec;28(12):1681-1693.
|
||
Epub 2020 Jul 31
|
||
doi: 10.1038/s41431-020-0678-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32737436" target="_blank">32737436</a><a href="/pmc/articles/PMC7784874" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29900826">Urothelial metaplasia of the seminal vesicle and ejaculatory duct associated with crossed-fused renal ectopia and Hutch diverticulum of the bladder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chezar K,
|
||
Gotto G,
|
||
Medlicott S,
|
||
Trpkov K</span><br />
|
||
<span class="medgenPMjournal">Can J Urol</span>
|
||
2018 Jun;25(3):9360-9362.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29900826" target="_blank">29900826</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Crossed%20fused%20renal%20ectopia%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 (3)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
||
|
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|
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|
||
|
||
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|
||
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|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
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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_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://clinicaltrials.gov/search?cond=Crossed%20fused%20renal%20ectopia" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
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|
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|
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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=(%22crossed%20fused%20renal%20ectopia%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=Crossed%20fused%20renal%20ectopia" target="_blank">MedlinePlus</a></li></ul></div>
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|
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<a href="/pubmed/clinical?term=Crossed%20fused%20renal%20ectopia" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Crossed%20fused%20renal%20ectopia%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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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=372130" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d53cf267c23b31e03f76b3">Crossed fused renal ectopia</a>
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||
<div class="ralinkpop offscreen_noflow">Crossed fused renal ectopia<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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</li>
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<li class="ra_rcd ralinkpopper two_line">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d53ce82f30673f7b845507">SALL4-Related Disorders - GeneReviews®</a>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d53ce784f3725e59c5b7a0">Table B. [OMIM Entries for SALL4-Related Disorders (View All in OMIM)]. - GeneRe...</a>
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<div class="ralinkpop offscreen_noflow">Table B. [OMIM Entries for SALL4-Related Disorders (View All in OMIM)]. - GeneReviews®<div class="brieflinkpopdesc"></div></div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=4" href="/portal/utils/pageresolver.fcgi?recordid=67d53ce684f3725e59c5b52f">Table A. [SALL4-Related Disorders: Genes and Databases]. - GeneReviews®</a>
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||
<div class="ralinkpop offscreen_noflow">Table A. [SALL4-Related Disorders: Genes and Databases]. - GeneReviews®<div class="brieflinkpopdesc"></div></div>
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