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<!--
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UID=140917
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ConceptID=C0431718
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Multiple renal cysts</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>140917</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.">C0431718</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>Multiple kidney cysts</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Multiple renal cysts (253883006)</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:0005562">HP:0005562</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">The presence of many cysts in the kidney. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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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">Multiple renal cysts</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/854361" ref="tree=MeSH" title="MedGen record for Renal cyst">Renal cyst</a></span><ul><li><span class="matched_ds">Multiple renal cysts</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_42458"><div><strong>Von Hippel-Lindau syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>42458</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.">C0019562</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Von Hippel-Lindau syndrome (VHL) is characterized by hemangioblastomas of the brain, spinal cord, and retina; renal cysts and clear cell renal cell carcinoma; pheochromocytoma and paraganglioma; pancreatic cysts and neuroendocrine tumors; endolymphatic sac tumors; and epididymal and broad ligament cystadenomas. Retinal hemangioblastomas may be the initial manifestation of VHL and can cause vision loss. Cerebellar hemangioblastomas may be associated with headache, vomiting, gait disturbances, or ataxia. Spinal hemangioblastomas and related syrinx usually present with pain. Sensory and motor loss may develop with cord compression. Renal cell carcinoma occurs in about 70% of individuals with VHL and is the leading cause of mortality. Pheochromocytomas can be asymptomatic but may cause sustained or episodic hypertension. Pancreatic lesions often remain asymptomatic and rarely cause endocrine or exocrine insufficiency. Endolymphatic sac tumors can cause hearing loss of varying severity, which can be a presenting symptom. Cystadenomas of the epididymis are relatively common. They rarely cause problems, unless bilateral, in which case they may result in infertility.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/42458">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_442699"><div><strong>Polycystic kidney disease 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>442699</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.">C2751306</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal dominant polycystic kidney disease (ADPKD) is generally a late-onset multisystem disorder characterized by bilateral kidney cysts, liver cysts, and an increased risk of intracranial aneurysms. Other manifestations include: cysts in the pancreas, seminal vesicles, and arachnoid membrane; dilatation of the aortic root and dissection of the thoracic aorta; mitral valve prolapse; and abdominal wall hernias. Kidney manifestations include early-onset hypertension, kidney pain, and kidney insufficiency. Approximately 50% of individuals with ADPKD have end-stage kidney disease (ESKD) by age 60 years. The prevalence of liver cysts increases with age and occasionally results in clinically significant severe polycystic liver disease (PLD), most often in females. Overall, the prevalence of intracranial aneurysms is fivefold higher than in the general population and further increased in those with a positive family history of aneurysms or subarachnoid hemorrhage. There is substantial variability in the severity of kidney disease and other extra-kidney manifestations.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/442699">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766914"><div><strong>Peroxisome biogenesis disorder 11A (Zellweger)</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766914</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.">C3554000</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Zellweger syndrome (ZS) is an autosomal recessive multiple congenital anomaly syndrome resulting from disordered peroxisome biogenesis. Affected children present in the newborn period with profound hypotonia, seizures, and inability to feed. Characteristic craniofacial anomalies, eye abnormalities, neuronal migration defects, hepatomegaly, and chondrodysplasia punctata are present. Children with this condition do not show any significant development and usually die in the first year of life (summary by Steinberg et al., 2006). For a complete phenotypic description and a discussion of genetic heterogeneity of Zellweger syndrome, see 214100. Individuals with PBDs of complementation group 13 (CG13, equivalent to CGH) have mutations in the PEX13 gene. For information on the history of PBD complementation groups, see 214100.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766914">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1381460"><div><strong>Immunoskeletal dysplasia with neurodevelopmental abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1381460</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.">C4479452</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/1381460">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684689"><div><strong>Neuromuscular disease and ocular or auditory anomalies with or without seizures</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684689</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.">C5231483</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neuromuscular oculoauditory syndrome (NMOAS) is a neurodevelopmental disorder with variable features including hypotonia, nonspecific developmental delay, and ear deformity or sensorineural deafness. Features may be reminiscent of Aicardi syndrome (see 304050), with chorioretinal lacunae, infantile spasms, and agenesis of the corpus callosum (Paine et al., 2019).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684689">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1823995"><div><strong>Polycystic kidney disease 7</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1823995</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.">C5774222</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal dominant polycystic kidney disease (ADPKD) is generally a late-onset multisystem disorder characterized by bilateral kidney cysts, liver cysts, and an increased risk of intracranial aneurysms. Other manifestations include: cysts in the pancreas, seminal vesicles, and arachnoid membrane; dilatation of the aortic root and dissection of the thoracic aorta; mitral valve prolapse; and abdominal wall hernias. Kidney manifestations include early-onset hypertension, kidney pain, and kidney insufficiency. Approximately 50% of individuals with ADPKD have end-stage kidney disease (ESKD) by age 60 years. The prevalence of liver cysts increases with age and occasionally results in clinically significant severe polycystic liver disease (PLD), most often in females. Overall, the prevalence of intracranial aneurysms is fivefold higher than in the general population and further increased in those with a positive family history of aneurysms or subarachnoid hemorrhage. There is substantial variability in the severity of kidney disease and other extra-kidney manifestations.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1823995">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1381460" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunoskeletal dysplasia with neurodevelopmental abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684689" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neuromuscular disease and ocular or auditory anomalies with or without seizures</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766914" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Peroxisome biogenesis disorder 11A (Zellweger)</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_442699" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Polycystic kidney disease 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1823995" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Polycystic kidney disease 7</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_42458" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Von Hippel-Lindau syndrome</a></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/38537868">Genotype-phenotype of autosomal dominant polycystic kidney disease in Malta.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ciantar N,
|
||
Zahra G,
|
||
Delicata J,
|
||
Sammut F,
|
||
Calleja-Agius J,
|
||
Farrugia E,
|
||
Said E</span><br />
|
||
<span class="medgenPMjournal">Eur J Med Genet</span>
|
||
2024 Jun;69:104934.
|
||
Epub 2024 Mar 26
|
||
doi: 10.1016/j.ejmg.2024.104934.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38537868" target="_blank">38537868</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35142283">Diagnosis and genotype-phenotype correlation in patients with PKD1/TSC2 contiguous gene deletion syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shang S,
|
||
Mei Y,
|
||
Wang T,
|
||
Zheng X,
|
||
Chen K,
|
||
Xiong S,
|
||
Dong Y,
|
||
Chang Y,
|
||
Wu X,
|
||
Kong X,
|
||
Tan M,
|
||
Wu L,
|
||
Zhang Y,
|
||
Xiao Y,
|
||
Xie Y,
|
||
Cai G,
|
||
Chen X,
|
||
Li Q</span><br />
|
||
<span class="medgenPMjournal">Clin Nephrol</span>
|
||
2022 Jun;97(6):328-338.
|
||
doi: 10.5414/CN110476.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35142283" target="_blank">35142283</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28623545">Analysis of genotypes and phenotypes in Chinese children with tuberous sclerosis complex.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bai D,
|
||
Zhao J,
|
||
Li L,
|
||
Gao J,
|
||
Wang X</span><br />
|
||
<span class="medgenPMjournal">Sci China Life Sci</span>
|
||
2017 Jul;60(7):763-771.
|
||
Epub 2017 Jun 14
|
||
doi: 10.1007/s11427-017-9091-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28623545" target="_blank">28623545</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22multiple%20renal%20cysts%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 (5)</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/38616607">Renal Pathology of Ciliopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sekar T,
|
||
Sebire NJ</span><br />
|
||
<span class="medgenPMjournal">Pediatr Dev Pathol</span>
|
||
2024 Sep-Oct;27(5):411-425.
|
||
Epub 2024 Apr 14
|
||
doi: 10.1177/10935266241242173.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38616607" target="_blank">38616607</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36030358">Association of multiple retinal nodular hamartomas and "confetti" skin lesions with end-stage renal disease in patients with tuberous sclerosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Prelevic V,
|
||
Juric I,
|
||
Bevc S,
|
||
Marcun-Varda N,
|
||
Aleckovic-Halilovic M,
|
||
Mesic E,
|
||
Bilic H,
|
||
Grujicic M,
|
||
Zabic I,
|
||
Josipovic J,
|
||
Vujicic B,
|
||
Marinaki S,
|
||
Simic-Ogrizovic S,
|
||
Milinkovic M,
|
||
Azasevac T,
|
||
Idrizi A,
|
||
Arnol M,
|
||
Radunovic D,
|
||
Antunovic T,
|
||
Jukic NB</span><br />
|
||
<span class="medgenPMjournal">Int Urol Nephrol</span>
|
||
2023 Feb;55(2):477-482.
|
||
Epub 2022 Aug 28
|
||
doi: 10.1007/s11255-022-03352-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36030358" target="_blank">36030358</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27577987">Novel association of familial testicular germ cell tumor and autosomal dominant polycystic kidney disease with PKD1 mutation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Truscott L,
|
||
Gell J,
|
||
Chang VY,
|
||
Lee H,
|
||
Strom SP,
|
||
Pillai R,
|
||
Sisk A,
|
||
Martinez-Agosto JA,
|
||
Anderson M,
|
||
Federman N</span><br />
|
||
<span class="medgenPMjournal">Pediatr Blood Cancer</span>
|
||
2017 Jan;64(1):100-102.
|
||
Epub 2016 Aug 31
|
||
doi: 10.1002/pbc.26197.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27577987" target="_blank">27577987</a><a href="/pmc/articles/PMC5937546" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22458902">Spectrum of preneoplastic and neoplastic cystic lesions of the kidney.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen YB,
|
||
Tickoo SK</span><br />
|
||
<span class="medgenPMjournal">Arch Pathol Lab Med</span>
|
||
2012 Apr;136(4):400-9.
|
||
doi: 10.5858/arpa.2011-0485-RA.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22458902" target="_blank">22458902</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/679518">Presymptomatic diagnosis of adult onset polycystic kidney disease by ultrasonography.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wolf B,
|
||
Rosenfield AT,
|
||
Taylor KJ,
|
||
Rosenfield N,
|
||
Gottlieb S,
|
||
Hsia YE</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
1978 Jul;14(1):1-7.
|
||
doi: 10.1111/j.1399-0004.1978.tb02053.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/679518" target="_blank">679518</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Multiple%20renal%20cysts%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 (25)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38616607">Renal Pathology of Ciliopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sekar T,
|
||
Sebire NJ</span><br />
|
||
<span class="medgenPMjournal">Pediatr Dev Pathol</span>
|
||
2024 Sep-Oct;27(5):411-425.
|
||
Epub 2024 Apr 14
|
||
doi: 10.1177/10935266241242173.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38616607" target="_blank">38616607</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30790041">A child with bilateral multiple renal cysts presenting with ascites and pleural effusion: Answers.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ağbaş A,
|
||
Aksu B,
|
||
Doğan G,
|
||
İkizceli T,
|
||
Selçuk HND,
|
||
Elevli M</span><br />
|
||
<span class="medgenPMjournal">Pediatr Nephrol</span>
|
||
2019 Sep;34(9):1543-1544.
|
||
Epub 2019 Feb 21
|
||
doi: 10.1007/s00467-019-4198-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30790041" target="_blank">30790041</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30790040">A child with bilateral multiple renal cysts presenting with ascites and pleural effusion: Questions.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ağbaş A,
|
||
Aksu B,
|
||
Doğan G,
|
||
İkizceli T,
|
||
Selçuk HND,
|
||
Elevli M</span><br />
|
||
<span class="medgenPMjournal">Pediatr Nephrol</span>
|
||
2019 Sep;34(9):1541-1542.
|
||
Epub 2019 Feb 21
|
||
doi: 10.1007/s00467-019-4196-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30790040" target="_blank">30790040</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25165175">How simple are 'simple renal cysts'?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Simms RJ,
|
||
Ong AC</span><br />
|
||
<span class="medgenPMjournal">Nephrol Dial Transplant</span>
|
||
2014 Sep;29 Suppl 4(Suppl 4):iv106-12.
|
||
doi: 10.1093/ndt/gfu106.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25165175" target="_blank">25165175</a><a href="/pmc/articles/PMC4158337" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18528323">A genetic syndrome of chronic renal failure with multiple renal cysts and early onset diabetes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Thomas CP,
|
||
Erlandson JC,
|
||
Edghill EL,
|
||
Hattersley AT,
|
||
Stolpen AH</span><br />
|
||
<span class="medgenPMjournal">Kidney Int</span>
|
||
2008 Oct;74(8):1094-9.
|
||
Epub 2008 Jun 4
|
||
doi: 10.1038/ki.2008.227.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18528323" target="_blank">18528323</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Multiple%20renal%20cysts%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 (66)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35031116">Oxygenated Hypothermic Machine Perfusion of Kidney Transplantation from Donors After Cardiac Death Due to Long-Term Low Blood Pressure and Hypoxia: The First Case Report of a Clinical Trial Using a New Japanese Perfusion System.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Miyagi S,
|
||
Kashiwadate T,
|
||
Nishimaki H,
|
||
Tokodai K,
|
||
Fujio A,
|
||
Miyazawa K,
|
||
Sasaki K,
|
||
Matsumura M,
|
||
Unno M,
|
||
Kamei T,
|
||
Matsuno N</span><br />
|
||
<span class="medgenPMjournal">Transplant Proc</span>
|
||
2022 Mar;54(2):225-229.
|
||
Epub 2022 Jan 11
|
||
doi: 10.1016/j.transproceed.2021.09.075.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35031116" target="_blank">35031116</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29019896">The efficacy of retroperitoneal laparoscopic deroofing of simple renal cyst with perirenal fat tissue wadding technique: A retrospective study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lai S,
|
||
Xu X,
|
||
Diao T,
|
||
Jiao B,
|
||
Jiang Z,
|
||
Zhang G</span><br />
|
||
<span class="medgenPMjournal">Medicine (Baltimore)</span>
|
||
2017 Oct;96(41):e8259.
|
||
doi: 10.1097/MD.0000000000008259.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29019896" target="_blank">29019896</a><a href="/pmc/articles/PMC5662319" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28260449">Living Kidney Donor Cancellation at King Hussein Medical Center.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Al-Rabadi K,
|
||
Almardini RI,
|
||
Hajeer M,
|
||
Hendawi M,
|
||
Hadad A</span><br />
|
||
<span class="medgenPMjournal">Exp Clin Transplant</span>
|
||
2017 Feb;15(Suppl 1):116-120.
|
||
doi: 10.6002/ect.mesot2016.O114.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28260449" target="_blank">28260449</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27577987">Novel association of familial testicular germ cell tumor and autosomal dominant polycystic kidney disease with PKD1 mutation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Truscott L,
|
||
Gell J,
|
||
Chang VY,
|
||
Lee H,
|
||
Strom SP,
|
||
Pillai R,
|
||
Sisk A,
|
||
Martinez-Agosto JA,
|
||
Anderson M,
|
||
Federman N</span><br />
|
||
<span class="medgenPMjournal">Pediatr Blood Cancer</span>
|
||
2017 Jan;64(1):100-102.
|
||
Epub 2016 Aug 31
|
||
doi: 10.1002/pbc.26197.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27577987" target="_blank">27577987</a><a href="/pmc/articles/PMC5937546" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6823908">Acquired renal cysts and multiple renal cell and urothelial tumors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chung-Park M,
|
||
Ricanati E,
|
||
Lankerani M,
|
||
Kedia K</span><br />
|
||
<span class="medgenPMjournal">Am J Clin Pathol</span>
|
||
1983 Feb;79(2):238-42.
|
||
doi: 10.1093/ajcp/79.2.238.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6823908" target="_blank">6823908</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Multiple%20renal%20cysts%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 (9)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35142283">Diagnosis and genotype-phenotype correlation in patients with PKD1/TSC2 contiguous gene deletion syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shang S,
|
||
Mei Y,
|
||
Wang T,
|
||
Zheng X,
|
||
Chen K,
|
||
Xiong S,
|
||
Dong Y,
|
||
Chang Y,
|
||
Wu X,
|
||
Kong X,
|
||
Tan M,
|
||
Wu L,
|
||
Zhang Y,
|
||
Xiao Y,
|
||
Xie Y,
|
||
Cai G,
|
||
Chen X,
|
||
Li Q</span><br />
|
||
<span class="medgenPMjournal">Clin Nephrol</span>
|
||
2022 Jun;97(6):328-338.
|
||
doi: 10.5414/CN110476.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35142283" target="_blank">35142283</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27577987">Novel association of familial testicular germ cell tumor and autosomal dominant polycystic kidney disease with PKD1 mutation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Truscott L,
|
||
Gell J,
|
||
Chang VY,
|
||
Lee H,
|
||
Strom SP,
|
||
Pillai R,
|
||
Sisk A,
|
||
Martinez-Agosto JA,
|
||
Anderson M,
|
||
Federman N</span><br />
|
||
<span class="medgenPMjournal">Pediatr Blood Cancer</span>
|
||
2017 Jan;64(1):100-102.
|
||
Epub 2016 Aug 31
|
||
doi: 10.1002/pbc.26197.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27577987" target="_blank">27577987</a><a href="/pmc/articles/PMC5937546" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23692786">Joubert syndrome: report of 11 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">İncecik F,
|
||
Hergüner MÖ,
|
||
Altunbaşak Ş,
|
||
Gleeson JG</span><br />
|
||
<span class="medgenPMjournal">Turk J Pediatr</span>
|
||
2012 Nov-Dec;54(6):605-11.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23692786" target="_blank">23692786</a><a href="/pmc/articles/PMC4442635" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22458902">Spectrum of preneoplastic and neoplastic cystic lesions of the kidney.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen YB,
|
||
Tickoo SK</span><br />
|
||
<span class="medgenPMjournal">Arch Pathol Lab Med</span>
|
||
2012 Apr;136(4):400-9.
|
||
doi: 10.5858/arpa.2011-0485-RA.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22458902" target="_blank">22458902</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18772274">Pictorial review of tuberous sclerosis in various organs.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Umeoka S,
|
||
Koyama T,
|
||
Miki Y,
|
||
Akai M,
|
||
Tsutsui K,
|
||
Togashi K</span><br />
|
||
<span class="medgenPMjournal">Radiographics</span>
|
||
2008 Nov-Dec;28(7):e32.
|
||
Epub 2008 Sep 4
|
||
doi: 10.1148/rg.e32.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18772274" target="_blank">18772274</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Multiple%20renal%20cysts%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 (20)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36442624">Inhibition of deubiquitinase USP28 attenuates cyst growth in autosomal dominant polycystic kidney disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ren Y,
|
||
Zhu X,
|
||
Fu K,
|
||
Zhang H,
|
||
Zhao W,
|
||
Lin Y,
|
||
Fang Q,
|
||
Wang J,
|
||
Chen Y,
|
||
Guo D</span><br />
|
||
<span class="medgenPMjournal">Biochem Pharmacol</span>
|
||
2023 Jan;207:115355.
|
||
Epub 2022 Nov 25
|
||
doi: 10.1016/j.bcp.2022.115355.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36442624" target="_blank">36442624</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28623545">Analysis of genotypes and phenotypes in Chinese children with tuberous sclerosis complex.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bai D,
|
||
Zhao J,
|
||
Li L,
|
||
Gao J,
|
||
Wang X</span><br />
|
||
<span class="medgenPMjournal">Sci China Life Sci</span>
|
||
2017 Jul;60(7):763-771.
|
||
Epub 2017 Jun 14
|
||
doi: 10.1007/s11427-017-9091-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28623545" target="_blank">28623545</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28260449">Living Kidney Donor Cancellation at King Hussein Medical Center.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Al-Rabadi K,
|
||
Almardini RI,
|
||
Hajeer M,
|
||
Hendawi M,
|
||
Hadad A</span><br />
|
||
<span class="medgenPMjournal">Exp Clin Transplant</span>
|
||
2017 Feb;15(Suppl 1):116-120.
|
||
doi: 10.6002/ect.mesot2016.O114.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28260449" target="_blank">28260449</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23692786">Joubert syndrome: report of 11 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">İncecik F,
|
||
Hergüner MÖ,
|
||
Altunbaşak Ş,
|
||
Gleeson JG</span><br />
|
||
<span class="medgenPMjournal">Turk J Pediatr</span>
|
||
2012 Nov-Dec;54(6):605-11.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23692786" target="_blank">23692786</a><a href="/pmc/articles/PMC4442635" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22458902">Spectrum of preneoplastic and neoplastic cystic lesions of the kidney.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen YB,
|
||
Tickoo SK</span><br />
|
||
<span class="medgenPMjournal">Arch Pathol Lab Med</span>
|
||
2012 Apr;136(4):400-9.
|
||
doi: 10.5858/arpa.2011-0485-RA.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22458902" target="_blank">22458902</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Multiple%20renal%20cysts%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 (20)</a></div></div>
|
||
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|
||
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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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|
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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_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Multiple%20renal%20cysts" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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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=(%22multiple%20renal%20cysts%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><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Multiple%20renal%20cysts%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. 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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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d598ffcde49f3df7087a5b">Multiple renal cysts</a>
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<div class="tertiary">MedGen</div>
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<div class="tertiary">MedGen</div>
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