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<meta name="keywords" content="C3808953, arhgdia, arhgdia nephrotic syndrome, disease or syndrome, nephrotic syndrome caused by mutation in arhgdia, nephrotic syndrome, type 8, nphs8, 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="Any nephrotic syndrome in which the cause of the disease is a mutation in the ARHGDIA gene." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
|
||
UID=815283
|
||
ConceptID=C3808953
|
||
-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Nephrotic syndrome, type 8<span class="h1sub">(NPHS8)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>815283</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:">C3808953</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>NPHS8</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Gene (location):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
|
||
Gene(s) directly associated with<br />
|
||
this condition or phenotype.</div></td>
|
||
<td><a target="_blank" title="ARHGDIA - ID: 396 - NCBI Gene" href="/gene/396" class="medgenPMinfo">ARHGDIA</a> (17q25.3)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0014099" target="_blank">MONDO:0014099</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/615244" target="_blank">615244</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 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">Any nephrotic syndrome in which the cause of the disease is a mutation in the ARHGDIA gene. [from <a title="Monarch Initiative" href="https://monarchinitiative.org/" class="defSource" target="_blank">MONDO</a>]</div>
|
||
</div>
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||
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<div class="portlet mgSection" id="ID_102">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
|
||
<div class="divPopper rprt" id="clin_10308"><div><strong>Nephrotic syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>10308</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.">C0027726</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Nephrotic syndrome is a collection of findings resulting from glomerular dysfunction with an increase in glomerular capillary wall permeability associated with pronounced proteinuria. Nephrotic syndrome refers to the constellation of clinical findings that result from severe renal loss of protein, with Proteinuria and hypoalbuminemia, edema, and hyperlipidemia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/10308">Feature record</a> | <a href="/medgen?term=%22Nephrotic%20syndrome%22%5BClinical%20Features%5D%20OR%2010308%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_10976"><div><strong>Proteinuria</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>10976</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.">C0033687</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Increased levels of protein in the urine.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/10976">Feature record</a> | <a href="/medgen?term=%22Proteinuria%22%5BClinical%20Features%5D%20OR%2010976%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_78698"><div><strong>Diffuse mesangial sclerosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>78698</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.">C0268747</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Diffuse sclerosis of the mesangium, as manifestated by diffuse mesangial matrix expansion.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/78698">Feature record</a> | <a href="/medgen?term=%22Diffuse%20mesangial%20sclerosis%22%5BClinical%20Features%5D%20OR%2078698%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_473458"><div><strong>Chronic kidney disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>473458</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.">C1561643</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Functional anomaly of the kidney persisting for at least three months.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/473458">Feature record</a> | <a href="/medgen?term=%22Chronic%20kidney%20disease%22%5BClinical%20Features%5D%20OR%20473458%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_384526"><div><strong>Stage 5 chronic kidney disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>384526</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.">C2316810</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A degree of kidney failure severe enough to require dialysis or kidney transplantation for survival characterized by a severe reduction in glomerular filtration rate (less than 15 ml/min/1.73 m2) and other manifestations including increased serum creatinine.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/384526">Feature record</a> | <a href="/medgen?term=%22Stage%205%20chronic%20kidney%20disease%22%5BClinical%20Features%5D%20OR%20384526%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_478451"><div><strong>Thin glomerular basement membrane</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>478451</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.">C3276821</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Decreased thickness of the glomerular basement membrane (GBM), measured from endothelial to visceral epithelial plasma membrane and mainly attributable to a decrease in thickness of the lamina densa, generally to an overall thickness more than 2 standard deviations less than that of the normal mean GBM thickness for health age- and sex matched individuals. May be focal or diffuse, although the term thin GBMs generally implies thinning of over 50% of GBMs.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/478451">Feature record</a> | <a href="/medgen?term=%22Thin%20glomerular%20basement%20membrane%22%5BClinical%20Features%5D%20OR%20478451%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_9164"><div><strong>Sensorineural hearing loss disorder</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>9164</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.">C0018784</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/9164">Feature record</a> | <a href="/medgen?term=%22Sensorineural%20hearing%20loss%20disorder%22%5BClinical%20Features%5D%20OR%209164%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_20693"><div><strong>Seizure</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>20693</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.">C0036572</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Sign or Symptom</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/20693">Feature record</a> | <a href="/medgen?term=%22Seizure%22%5BClinical%20Features%5D%20OR%2020693%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_811461"><div><strong>Intellectual disability</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>811461</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.">C3714756</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Intellectual disability, previously referred to as mental retardation, is characterized by subnormal intellectual functioning that occurs during the developmental period. It is defined by an IQ score below 70.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/811461">Feature record</a> | <a href="/medgen?term=%22Intellectual%20disability%22%5BClinical%20Features%5D%20OR%20811461%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_4451"><div><strong>Edema</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>4451</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.">C0013604</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/4451">Feature record</a> | <a href="/medgen?term=%22Edema%22%5BClinical%20Features%5D%20OR%204451%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_68694"><div><strong>Hypoalbuminemia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>68694</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.">C0239981</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Reduction in the concentration of albumin in the blood.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/68694">Feature record</a> | <a href="/medgen?term=%22Hypoalbuminemia%22%5BClinical%20Features%5D%20OR%2068694%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_376817"><div><strong>Generalized edema</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>376817</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.">C1850534</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Generalized abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/376817">Feature record</a> | <a href="/medgen?term=%22Generalized%20edema%22%5BClinical%20Features%5D%20OR%20376817%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_890568"><div><strong>Cerebral visual impairment</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>890568</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.">C4048268</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A form of loss of vision caused by damage to the visual cortex rather than a defect in the eye.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/890568">Feature record</a> | <a href="/medgen?term=%22Cerebral%20visual%20impairment%22%5BClinical%20Features%5D%20OR%20890568%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite" data-jigconfig="closed: 1"><div class="concept-def"><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().openAll(); return false;">Show all</a><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().closeAll(); return false;">Hide all</a></div><ul><li><span class="TLline">Abnormality of metabolism/homeostasis</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_4451" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Edema</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_376817" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Generalized edema</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_68694" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypoalbuminemia</a></span></li></ul></li><li><span class="TLline">Abnormality of the eye</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_890568" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebral visual impairment</a></span></li></ul></li><li><span class="TLline">Abnormality of the genitourinary system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_473458" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chronic kidney disease</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_78698" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Diffuse mesangial sclerosis</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_10308" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nephrotic syndrome</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_10976" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Proteinuria</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_384526" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Stage 5 chronic kidney disease</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_478451" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Thin glomerular basement membrane</a></span></li></ul></li><li><span class="TLline">Abnormality of the nervous system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_811461" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_20693" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Seizure</a></span></li></ul></li><li><span class="TLline">Ear malformation</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_9164" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Sensorineural hearing loss disorder</a></span></li></ul></li></ul></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/33854215">Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Savige J,
|
||
Storey H,
|
||
Watson E,
|
||
Hertz JM,
|
||
Deltas C,
|
||
Renieri A,
|
||
Mari F,
|
||
Hilbert P,
|
||
Plevova P,
|
||
Byers P,
|
||
Cerkauskaite A,
|
||
Gregory M,
|
||
Cerkauskiene R,
|
||
Ljubanovic DG,
|
||
Becherucci F,
|
||
Errichiello C,
|
||
Massella L,
|
||
Aiello V,
|
||
Lennon R,
|
||
Hopkinson L,
|
||
Koziell A,
|
||
Lungu A,
|
||
Rothe HM,
|
||
Hoefele J,
|
||
Zacchia M,
|
||
Martic TN,
|
||
Gupta A,
|
||
van Eerde A,
|
||
Gear S,
|
||
Landini S,
|
||
Palazzo V,
|
||
Al-Rabadi L,
|
||
Claes K,
|
||
Corveleyn A,
|
||
Van Hoof E,
|
||
van Geel M,
|
||
Williams M,
|
||
Ashton E,
|
||
Belge H,
|
||
Ars E,
|
||
Bierzynska A,
|
||
Gangemi C,
|
||
Lipska-Ziętkiewicz BS</span><br />
|
||
<span class="medgenPMjournal">Eur J Hum Genet</span>
|
||
2021 Aug;29(8):1186-1197.
|
||
Epub 2021 Apr 15
|
||
doi: 10.1038/s41431-021-00858-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33854215" target="_blank">33854215</a><a href="/pmc/articles/PMC8384871" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33684950">Clinical Analysis of Primary Nephrotic Syndrome Complicated by Plastic Bronchitis in Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jia SL,
|
||
Ni FF,
|
||
Ma YJ,
|
||
Wu YH,
|
||
Ma WK,
|
||
Gao XJ</span><br />
|
||
<span class="medgenPMjournal">Klin Padiatr</span>
|
||
2021 Mar;233(2):63-68.
|
||
Epub 2021 Mar 8
|
||
doi: 10.1055/a-1288-3670.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33684950" target="_blank">33684950</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33581711">Rituximab treatment for difficult-to-treat nephrotic syndrome in children: a multicenter, retrospective study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Taşdemir M,
|
||
Canpolat N,
|
||
Yıldız N,
|
||
Özçelik G,
|
||
Benzer M,
|
||
Saygılı SK,
|
||
Özkayin EN,
|
||
Türkkan ÖN,
|
||
Balat A,
|
||
Candan C,
|
||
Çelakıl M,
|
||
Yavuz S,
|
||
Akıncı N,
|
||
Göknar N,
|
||
Akgün C,
|
||
Tülpar S,
|
||
Alpay H,
|
||
Sever FL,
|
||
Bilge İ</span><br />
|
||
<span class="medgenPMjournal">Turk J Med Sci</span>
|
||
2021 Aug 30;51(4):1781-1790.
|
||
doi: 10.3906/sag-2012-297.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33581711" target="_blank">33581711</a><a href="/pmc/articles/PMC8569731" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(nephrotic%20syndrome%2C%20type%208)%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 (17)</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/38453268">A Low-Protein, Plant-Dominant Gluten-Free Diet for Immunoglobulin A Nephropathy and Focal Segmental Glomerulosclerosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Patel J,
|
||
Kalantar-Zadeh K,
|
||
Betz M,
|
||
Joshi S</span><br />
|
||
<span class="medgenPMjournal">Adv Kidney Dis Health</span>
|
||
2023 Nov;30(6):517-522.
|
||
doi: 10.1053/j.akdh.2023.09.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38453268" target="_blank">38453268</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38250076">Clinicopathological and prognostic characteristics of idiopathic membranous nephropathy with dual antigen positivity.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yang L,
|
||
Wang G,
|
||
Ye N,
|
||
Xu X,
|
||
Cheng W,
|
||
Sun L,
|
||
Dong H,
|
||
Kong L,
|
||
Zhao X,
|
||
Geng Y,
|
||
Cheng H</span><br />
|
||
<span class="medgenPMjournal">Front Immunol</span>
|
||
2023;14:1297107.
|
||
Epub 2024 Jan 5
|
||
doi: 10.3389/fimmu.2023.1297107.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38250076" target="_blank">38250076</a><a href="/pmc/articles/PMC10796489" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35224732">Interventions for focal segmental glomerulosclerosis in adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hodson EM,
|
||
Sinha A,
|
||
Cooper TE</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2022 Feb 28;2(2):CD003233.
|
||
doi: 10.1002/14651858.CD003233.pub3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35224732" target="_blank">35224732</a><a href="/pmc/articles/PMC8883337" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33833079">Protocadherin 7-Associated Membranous Nephropathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sethi S,
|
||
Madden B,
|
||
Debiec H,
|
||
Morelle J,
|
||
Charlesworth MC,
|
||
Gross L,
|
||
Negron V,
|
||
Buob D,
|
||
Chaudhry S,
|
||
Jadoul M,
|
||
Fervenza FC,
|
||
Ronco P</span><br />
|
||
<span class="medgenPMjournal">J Am Soc Nephrol</span>
|
||
2021 May 3;32(5):1249-1261.
|
||
Epub 2021 Apr 8
|
||
doi: 10.1681/ASN.2020081165.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33833079" target="_blank">33833079</a><a href="/pmc/articles/PMC8259689" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32447467">Renal amyloidosis: an update on diagnosis and pathogenesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gupta N,
|
||
Kaur H,
|
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Wajid S</span><br />
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<span class="medgenPMjournal">Protoplasma</span>
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2020 Sep;257(5):1259-1276.
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Epub 2020 May 24
|
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doi: 10.1007/s00709-020-01513-0.
|
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<span class="bold">PMID: </span><a href="/pubmed/32447467" target="_blank">32447467</a></div>
|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Nephrotic%20syndrome%2C%20type%208%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 (184)</a></div><h3 class="subhead">Diagnosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/33854215">Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Savige J,
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Lennon R,
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Martic TN,
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Gupta A,
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van Eerde A,
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Gear S,
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Palazzo V,
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Williams M,
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Ashton E,
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Belge H,
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<span class="medgenPMjournal">Eur J Hum Genet</span>
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2021 Aug;29(8):1186-1197.
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<span class="bold">PMID: </span><a href="/pubmed/33854215" target="_blank">33854215</a><a href="/pmc/articles/PMC8384871" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32447467">Renal amyloidosis: an update on diagnosis and pathogenesis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Gupta N,
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Kaur H,
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Wajid S</span><br />
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<span class="medgenPMjournal">Protoplasma</span>
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2020 Sep;257(5):1259-1276.
|
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Epub 2020 May 24
|
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doi: 10.1007/s00709-020-01513-0.
|
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<span class="bold">PMID: </span><a href="/pubmed/32447467" target="_blank">32447467</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32423387">Glomerulonephritis Histopathological Pattern Change.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">AlYousef A,
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AlSahow A,
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AlHelal B,
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Alqallaf A,
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Abdallah E,
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Abdellatif M,
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2020 May 18;21(1):186.
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<span class="bold">PMID: </span><a href="/pubmed/32423387" target="_blank">32423387</a><a href="/pmc/articles/PMC7236312" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/30683678">Primary membranous nephropathy: comprehensive review and historical perspective.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Keri KC,
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Blumenthal S,
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Kulkarni V,
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Beck L,
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2019 Jan;95(1119):23-31.
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<span class="bold">PMID: </span><a href="/pubmed/30683678" target="_blank">30683678</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/30183397">Familial Chylomicronemia Syndrome: A Clinical Guide For Endocrinologists.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Falko JM</span><br />
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2018 Aug;24(8):756-763.
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<span class="bold">PMID: </span><a href="/pubmed/30183397" target="_blank">30183397</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Nephrotic%20syndrome%2C%20type%208%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 (191)</a></div><h3 class="subhead">Therapy</h3>
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<div class="nl"><a target="_blank" href="/pubmed/38453268">A Low-Protein, Plant-Dominant Gluten-Free Diet for Immunoglobulin A Nephropathy and Focal Segmental Glomerulosclerosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Patel J,
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<span class="bold">PMID: </span><a href="/pubmed/38453268" target="_blank">38453268</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Soares LR,
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Jorge LB,
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<span class="medgenPMjournal">Braz J Med Biol Res</span>
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<span class="bold">PMID: </span><a href="/pubmed/35239780" target="_blank">35239780</a><a href="/pmc/articles/PMC8905670" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/35224732">Interventions for focal segmental glomerulosclerosis in adults.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Hodson EM,
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Sinha A,
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<div class="nl"><a target="_blank" href="/pubmed/30683678">Primary membranous nephropathy: comprehensive review and historical perspective.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Keri KC,
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Blumenthal S,
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Kulkarni V,
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Beck L,
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Chongkrairatanakul T</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/30683678" target="_blank">30683678</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Feng M,
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Yuan W,
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Zhang R,
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<span class="bold">PMID: </span><a href="/pubmed/23740567" target="_blank">23740567</a><a href="/pmc/articles/PMC11380091" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Nephrotic%20syndrome%2C%20type%208%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 (139)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/38250076">Clinicopathological and prognostic characteristics of idiopathic membranous nephropathy with dual antigen positivity.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Yang L,
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Wang G,
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Ye N,
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Xu X,
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Cheng W,
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Sun L,
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Dong H,
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Kong L,
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Zhao X,
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<span class="bold">PMID: </span><a href="/pubmed/38250076" target="_blank">38250076</a><a href="/pmc/articles/PMC10796489" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/32447467">Renal amyloidosis: an update on diagnosis and pathogenesis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Gupta N,
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Kaur H,
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Wajid S</span><br />
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<span class="medgenPMjournal">Protoplasma</span>
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2020 Sep;257(5):1259-1276.
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Epub 2020 May 24
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doi: 10.1007/s00709-020-01513-0.
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<span class="bold">PMID: </span><a href="/pubmed/32447467" target="_blank">32447467</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32423387">Glomerulonephritis Histopathological Pattern Change.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">AlYousef A,
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AlSahow A,
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AlHelal B,
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Alqallaf A,
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Abdallah E,
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Abdellatif M,
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Nawar H,
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Elmahalawy R</span><br />
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<span class="medgenPMjournal">BMC Nephrol</span>
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2020 May 18;21(1):186.
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doi: 10.1186/s12882-020-01836-3.
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<span class="bold">PMID: </span><a href="/pubmed/32423387" target="_blank">32423387</a><a href="/pmc/articles/PMC7236312" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/30683678">Primary membranous nephropathy: comprehensive review and historical perspective.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Keri KC,
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Blumenthal S,
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Kulkarni V,
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Beck L,
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Chongkrairatanakul T</span><br />
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<span class="medgenPMjournal">Postgrad Med J</span>
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2019 Jan;95(1119):23-31.
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Epub 2019 Jan 25
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<span class="bold">PMID: </span><a href="/pubmed/30683678" target="_blank">30683678</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28949280">Childhood nephrotic syndrome in tropical Africa: then and now.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Olowu WA,
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Ademola A,
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Ajite AB,
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<span class="medgenPMjournal">Paediatr Int Child Health</span>
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2017 Nov;37(4):259-268.
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<span class="bold">PMID: </span><a href="/pubmed/28949280" target="_blank">28949280</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Nephrotic%20syndrome%2C%20type%208%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 (136)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37907612">Exploring the significance of interleukin-33/ST2 axis in minimal change disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Kanazawa N,
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Iyoda M,
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<span class="bold">PMID: </span><a href="/pubmed/37907612" target="_blank">37907612</a><a href="/pmc/articles/PMC10618262" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/37881096">Clinical and pathological features of omicron variant of SARS-CoV-2-associated kidney injury.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Qi Z,
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Yuan S,
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Wei J,
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Xia S,
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Huang Y,
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Chen X,
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Han Y,
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Li Z,
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Xiao Y,
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Peng F,
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Fu X,
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<span class="bold">PMID: </span><a href="/pubmed/37881096" target="_blank">37881096</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32423387">Glomerulonephritis Histopathological Pattern Change.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">AlYousef A,
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AlSahow A,
|
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AlHelal B,
|
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Alqallaf A,
|
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Abdallah E,
|
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Abdellatif M,
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Nawar H,
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Elmahalawy R</span><br />
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<span class="medgenPMjournal">BMC Nephrol</span>
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2020 May 18;21(1):186.
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doi: 10.1186/s12882-020-01836-3.
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<span class="bold">PMID: </span><a href="/pubmed/32423387" target="_blank">32423387</a><a href="/pmc/articles/PMC7236312" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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<div class="nl"><a target="_blank" href="/pubmed/31015507">The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Li LZ,
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Hu Y,
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Ai SL,
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Cheng L,
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Liu J,
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|
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<div class="nl"><a target="_blank" href="/pubmed/28614261">A PRISMA-compliant meta-analysis of MDR1 polymorphisms and idiopathic nephrotic syndrome: Susceptibility and steroid responsiveness.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Han SS,
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Xu YQ,
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Lu Y,
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<span class="medgenPMjournal">Medicine (Baltimore)</span>
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<span class="bold">PMID: </span><a href="/pubmed/28614261" target="_blank">28614261</a><a href="/pmc/articles/PMC5478346" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Nephrotic%20syndrome%2C%20type%208%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 (119)</a></div></div>
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</div>
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|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln">
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<div class="nl"><a target="_blank" href="/pubmed/38965515">Nephrotic syndrome associated with solid malignancies: a systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Liu S,
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Wan Y,
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Hu Z,
|
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Wang Z,
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Liu F</span><br />
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<span class="medgenPMjournal">BMC Nephrol</span>
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2024 Jul 4;25(1):215.
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doi: 10.1186/s12882-024-03632-9.
|
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<span class="bold">PMID: </span><a href="/pubmed/38965515" target="_blank">38965515</a><a href="/pmc/articles/PMC11225115" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/36371483">Sphingosine phosphate lyase insufficiency syndrome: a systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Pournasiri Z,
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Madani A,
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Nazarpack F,
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Sayer JA,
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Chavoshzadeh Z,
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Nili F,
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Tran P,
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Saba JD,
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Jamee M</span><br />
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<span class="medgenPMjournal">World J Pediatr</span>
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2023 May;19(5):425-437.
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Epub 2022 Nov 12
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<span class="bold">PMID: </span><a href="/pubmed/36371483" target="_blank">36371483</a></div>
|
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|
||
<div class="nl"><a target="_blank" href="/pubmed/35224732">Interventions for focal segmental glomerulosclerosis in adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hodson EM,
|
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Sinha A,
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Cooper TE</span><br />
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<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
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2022 Feb 28;2(2):CD003233.
|
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doi: 10.1002/14651858.CD003233.pub3.
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<span class="bold">PMID: </span><a href="/pubmed/35224732" target="_blank">35224732</a><a href="/pmc/articles/PMC8883337" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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|
||
<div class="nl"><a target="_blank" href="/pubmed/23740567">Chinese herbal medicine Huangqi type formulations for nephrotic syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Feng M,
|
||
Yuan W,
|
||
Zhang R,
|
||
Fu P,
|
||
Wu T</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2013 Jun 5;2013(6):CD006335.
|
||
doi: 10.1002/14651858.CD006335.pub3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23740567" target="_blank">23740567</a><a href="/pmc/articles/PMC11380091" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20538785">Bevacizumab increases risk for severe proteinuria in cancer patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wu S,
|
||
Kim C,
|
||
Baer L,
|
||
Zhu X</span><br />
|
||
<span class="medgenPMjournal">J Am Soc Nephrol</span>
|
||
2010 Aug;21(8):1381-9.
|
||
Epub 2010 Jun 10
|
||
doi: 10.1681/ASN.2010020167.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20538785" target="_blank">20538785</a><a href="/pmc/articles/PMC2938590" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Nephrotic%20syndrome%2C%20type%208%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (6)</a></div></div>
|
||
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|
||
</div></div></div></div></div></div></div>
|
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<div class="supplemental col three_col last">
|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C3808953%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (12)</a></li>
|
||
<li><a href="/gtr/tests?term=C3808953%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (19)</a></li>
|
||
<li><a href="/gtr/tests?term=C3808953%5bDISCUI%5d&filter=method%3A2%5F19" target="_blank">Targeted variant analysis (7)</a></li>
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<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C3808953%5bDISCUI%5d" target="_blank">See all (21)</a></total></li>
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