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<meta name="keywords" content="C5421632, finding, renal cortical hyperechogenicity, 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="Increased echogenecity of the kidney cortex." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=1770764
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ConceptID=C5421632
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Renal cortical hyperechogenicity</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1770764</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:">C5421632</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><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:0033132">HP:0033132</a></td></tr>
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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">Increased echogenecity of the kidney cortex. [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="TLline">Renal cortical hyperechogenicity</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/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/1723255" ref="tree=MeSH" title="MedGen record for Abnormal renal echogenicity">Abnormal renal echogenicity</a></span><ul><li><span class="matched_ds">Renal cortical hyperechogenicity</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
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||
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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>
|
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<div class="portlet_content ln clinfeat">
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||
<div class="divPopper rprt" id="rdis_141632"><div><strong>Dalmatian hypouricemia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141632</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.">C0473219</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Renal hypouricemia is characterized by impaired uric acid reabsorption at the apical membrane of proximal renal tubule cells. The syndrome is not lethal and may be asymptomatic. However, it is accompanied by nephrolithiasis and exercise-induced acute renal failure in about 10% of patients (Ichida et al., 2008). Genetic Heterogeneity of Renal Hypouricemia See also RHUC2 (612076), which is caused by mutation in the SLC2A9 gene (606142).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/141632">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_370587"><div><strong>Renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>370587</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.">C1969055</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/370587">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1781068"><div><strong>Nephrotic syndrome, type 24</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1781068</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.">C5543267</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Nephrotic syndrome type 24 (NPHS24) is an autosomal recessive renal disorder characterized by onset of proteinuria and hypoalbuminemia in early childhood, although onset in the second decade has been reported. Additional features include edema and hyperlipidemia. The disorder is slowly progressive, and most patients eventually develop end-stage renal disease. Renal biopsy shows focal segmental glomerulosclerosis (FSGS) (summary by Schneider et al., 2020). For a general phenotypic description and a discussion of genetic heterogeneity of nephrotic syndrome, see NPHS1 (256300).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1781068">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1788773"><div><strong>Megacystis-microcolon-intestinal hypoperistalsis syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1788773</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.">C5543476</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Megacystis-microcolon-intestinal hypoperistalsis syndrome-2 (MMIHS2) is characterized by prenatal bladder enlargement, neonatal functional gastrointestinal obstruction, and chronic dependence on total parenteral nutrition and urinary catheterization. The majority of cases have a fatal outcome due to malnutrition and sepsis, followed by multiorgan failure (summary by Wang et al., 2019). For a discussion of genetic heterogeneity of MMIHS, see 249210.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1788773">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1847314"><div><strong>Yuksel-Vogel-Bauer syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1847314</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.">C5882751</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Yuksel-Vogel-Bauer syndrome (YUVOB) is a multisystemic disorder characterized by variable congenital defects involving the brain, kidney, heart, and/or skeletal system. Features may include hydrocephalus, developmental delay, cleft lip/palate, cystic renal dysplasia or tubular leak, cardiac septal defects, and broad hands and feet (Yuksel et al., 2019; Marquez et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1847314">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_141632" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Dalmatian hypouricemia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1788773" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Megacystis-microcolon-intestinal hypoperistalsis syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1781068" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nephrotic syndrome, type 24</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_370587" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1847314" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Yuksel-Vogel-Bauer syndrome</a></div></div>
|
||
</div>
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||
|
||
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<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/12736757">The contribution of ultrasound for the differential diagnosis of congenital and infantile nephrotic syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Salame H,
|
||
Damry N,
|
||
Vandenhoudt K,
|
||
Hall M,
|
||
Avni FE</span><br />
|
||
<span class="medgenPMjournal">Eur Radiol</span>
|
||
2003 Dec;13(12):2674-9.
|
||
Epub 2003 May 8
|
||
doi: 10.1007/s00330-003-1920-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12736757" target="_blank">12736757</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(renal%20cortical%20hyperechogenicity)%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/37057397">Ultrasound Patterns and Disease Progression in Medullary Sponge Kidney in Adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gliga ML,
|
||
Chirila C,
|
||
Chirila PM</span><br />
|
||
<span class="medgenPMjournal">Ultrason Imaging</span>
|
||
2023 May;45(3):151-155.
|
||
Epub 2023 Apr 14
|
||
doi: 10.1177/01617346231165493.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37057397" target="_blank">37057397</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36746811">Imaging findings of COPA Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nguyen HN,
|
||
Salman R,
|
||
Vogel TP,
|
||
Silva-Carmona M,
|
||
DeGuzman M,
|
||
Guillerman RP</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
2023 May;53(5):844-853.
|
||
Epub 2023 Feb 7
|
||
doi: 10.1007/s00247-023-05600-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36746811" target="_blank">36746811</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29159839">Increased Renal Echogenicity in Children With Appendicitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tal Tamir H,
|
||
Ben-Mordechay D,
|
||
Ben-Shlush A,
|
||
Raviv-Zilka L,
|
||
Soudack M</span><br />
|
||
<span class="medgenPMjournal">J Ultrasound Med</span>
|
||
2018 Jun;37(6):1403-1409.
|
||
Epub 2017 Nov 21
|
||
doi: 10.1002/jum.14480.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29159839" target="_blank">29159839</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16869009">Relationship of increased renal cortical echogenicity with clinical and laboratory findings in pediatric renal disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kasap B,
|
||
Soylu A,
|
||
Türkmen M,
|
||
Kavukcu S</span><br />
|
||
<span class="medgenPMjournal">J Clin Ultrasound</span>
|
||
2006 Sep;34(7):339-42.
|
||
doi: 10.1002/jcu.20243.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16869009" target="_blank">16869009</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11548184">Renal injury in perinatal hypoxia: ultrasonography and changes in renal function.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Streitman K,
|
||
Tóth A,
|
||
Horváth I,
|
||
Tálosi G</span><br />
|
||
<span class="medgenPMjournal">Eur J Pediatr</span>
|
||
2001 Aug;160(8):473-7.
|
||
doi: 10.1007/s004310100769.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11548184" target="_blank">11548184</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%20hyperechogenicity%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 (15)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37057397">Ultrasound Patterns and Disease Progression in Medullary Sponge Kidney in Adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gliga ML,
|
||
Chirila C,
|
||
Chirila PM</span><br />
|
||
<span class="medgenPMjournal">Ultrason Imaging</span>
|
||
2023 May;45(3):151-155.
|
||
Epub 2023 Apr 14
|
||
doi: 10.1177/01617346231165493.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37057397" target="_blank">37057397</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29159839">Increased Renal Echogenicity in Children With Appendicitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tal Tamir H,
|
||
Ben-Mordechay D,
|
||
Ben-Shlush A,
|
||
Raviv-Zilka L,
|
||
Soudack M</span><br />
|
||
<span class="medgenPMjournal">J Ultrasound Med</span>
|
||
2018 Jun;37(6):1403-1409.
|
||
Epub 2017 Nov 21
|
||
doi: 10.1002/jum.14480.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29159839" target="_blank">29159839</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28730376">Lower urinary tract obstruction: fetal intervention based on prenatal staging.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ruano R,
|
||
Dunn T,
|
||
Braun MC,
|
||
Angelo JR,
|
||
Safdar A</span><br />
|
||
<span class="medgenPMjournal">Pediatr Nephrol</span>
|
||
2017 Oct;32(10):1871-1878.
|
||
Epub 2017 Jul 21
|
||
doi: 10.1007/s00467-017-3593-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28730376" target="_blank">28730376</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27169608">Clinical Scenarios in Chronic Kidney Disease: Chronic Tubulointerstitial Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Meola M,
|
||
Samoni S,
|
||
Petrucci I</span><br />
|
||
<span class="medgenPMjournal">Contrib Nephrol</span>
|
||
2016;188:108-19.
|
||
Epub 2016 May 12
|
||
doi: 10.1159/000445473.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27169608" target="_blank">27169608</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8518103">Hyperechoic kidneys in the newborn and young infant.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Slovis TL,
|
||
Bernstein J,
|
||
Gruskin A</span><br />
|
||
<span class="medgenPMjournal">Pediatr Nephrol</span>
|
||
1993 Jun;7(3):294-302.
|
||
doi: 10.1007/BF00853228.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8518103" target="_blank">8518103</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%20hyperechogenicity%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 (28)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29193639">Oligonephronia and Wolf-Hirschhorn syndrome: A further observation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gatto A,
|
||
Ferrara P,
|
||
Leoni C,
|
||
Onesimo R,
|
||
Zollino M,
|
||
Emma F,
|
||
Zampino G</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2018 Feb;176(2):409-414.
|
||
Epub 2017 Nov 28
|
||
doi: 10.1002/ajmg.a.38554.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29193639" target="_blank">29193639</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7658265">Uroradiologic evaluation of children with urinary tract infection: are both ultrasonograpy and renal cortical scintigraphy necessary?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sreenarasimhaiah V,
|
||
Alon US</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
1995 Sep;127(3):373-7.
|
||
doi: 10.1016/s0022-3476(95)70066-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7658265" target="_blank">7658265</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%20hyperechogenicity%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 (2)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37057397">Ultrasound Patterns and Disease Progression in Medullary Sponge Kidney in Adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gliga ML,
|
||
Chirila C,
|
||
Chirila PM</span><br />
|
||
<span class="medgenPMjournal">Ultrason Imaging</span>
|
||
2023 May;45(3):151-155.
|
||
Epub 2023 Apr 14
|
||
doi: 10.1177/01617346231165493.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37057397" target="_blank">37057397</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28730376">Lower urinary tract obstruction: fetal intervention based on prenatal staging.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ruano R,
|
||
Dunn T,
|
||
Braun MC,
|
||
Angelo JR,
|
||
Safdar A</span><br />
|
||
<span class="medgenPMjournal">Pediatr Nephrol</span>
|
||
2017 Oct;32(10):1871-1878.
|
||
Epub 2017 Jul 21
|
||
doi: 10.1007/s00467-017-3593-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28730376" target="_blank">28730376</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27401742">Posterior urethral valves: are neonatal imaging findings predictive of renal function during early childhood?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hochart V,
|
||
Lahoche A,
|
||
Priso RH,
|
||
Houfflin-Debarge V,
|
||
Bassil A,
|
||
Sharma D,
|
||
Behal H,
|
||
Avni FE</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
2016 Sep;46(10):1418-23.
|
||
Epub 2016 Jul 11
|
||
doi: 10.1007/s00247-016-3634-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27401742" target="_blank">27401742</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16450351">Prenatal findings in four consecutive pregnancies with fetal Pierson syndrome, a newly defined congenital nephrosis syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mark K,
|
||
Reis A,
|
||
Zenker M</span><br />
|
||
<span class="medgenPMjournal">Prenat Diagn</span>
|
||
2006 Mar;26(3):262-6.
|
||
doi: 10.1002/pd.1393.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16450351" target="_blank">16450351</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15229917">Prenatal sonographic patterns in autosomal dominant polycystic kidney disease: a multicenter study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Brun M,
|
||
Maugey-Laulom B,
|
||
Eurin D,
|
||
Didier F,
|
||
Avni EF</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
|
||
2004 Jul;24(1):55-61.
|
||
doi: 10.1002/uog.1098.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15229917" target="_blank">15229917</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%20hyperechogenicity%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/37057397">Ultrasound Patterns and Disease Progression in Medullary Sponge Kidney in Adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gliga ML,
|
||
Chirila C,
|
||
Chirila PM</span><br />
|
||
<span class="medgenPMjournal">Ultrason Imaging</span>
|
||
2023 May;45(3):151-155.
|
||
Epub 2023 Apr 14
|
||
doi: 10.1177/01617346231165493.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37057397" target="_blank">37057397</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31659787">Prediction model of postnatal renal function in fetuses with lower urinary tract obstruction (LUTO)-Development and internal validation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Duin LK,
|
||
Fontanella F,
|
||
Groen H,
|
||
Adama van Scheltema PN,
|
||
Cohen-Overbeek TE,
|
||
Pajkrt E,
|
||
Bekker M,
|
||
Willekes C,
|
||
Bax CJ,
|
||
Oepkes D,
|
||
Bilardo CM</span><br />
|
||
<span class="medgenPMjournal">Prenat Diagn</span>
|
||
2019 Dec;39(13):1235-1241.
|
||
Epub 2019 Oct 28
|
||
doi: 10.1002/pd.5573.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31659787" target="_blank">31659787</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30791938">Not only Alagille syndrome. Syndromic paucity of interlobular bile ducts secondary to HNF1β deficiency: a case report and literature review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pinon M,
|
||
Carboni M,
|
||
Colavito D,
|
||
Cisarò F,
|
||
Peruzzi L,
|
||
Pizzol A,
|
||
Calosso G,
|
||
David E,
|
||
Calvo PL</span><br />
|
||
<span class="medgenPMjournal">Ital J Pediatr</span>
|
||
2019 Feb 21;45(1):27.
|
||
doi: 10.1186/s13052-019-0617-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30791938" target="_blank">30791938</a><a href="/pmc/articles/PMC6385394" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29193639">Oligonephronia and Wolf-Hirschhorn syndrome: A further observation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gatto A,
|
||
Ferrara P,
|
||
Leoni C,
|
||
Onesimo R,
|
||
Zollino M,
|
||
Emma F,
|
||
Zampino G</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2018 Feb;176(2):409-414.
|
||
Epub 2017 Nov 28
|
||
doi: 10.1002/ajmg.a.38554.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29193639" target="_blank">29193639</a></div>
|
||
|
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<div class="nl"><a target="_blank" href="/pubmed/27401742">Posterior urethral valves: are neonatal imaging findings predictive of renal function during early childhood?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hochart V,
|
||
Lahoche A,
|
||
Priso RH,
|
||
Houfflin-Debarge V,
|
||
Bassil A,
|
||
Sharma D,
|
||
Behal H,
|
||
Avni FE</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
2016 Sep;46(10):1418-23.
|
||
Epub 2016 Jul 11
|
||
doi: 10.1007/s00247-016-3634-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27401742" target="_blank">27401742</a></div>
|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%20hyperechogenicity%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 (14)</a></div></div>
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