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<!--
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UID=370605
|
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ConceptID=C1969144
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Renal cortical cysts</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>370605</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.">C1969144</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Cortical cysts</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:0000803">HP:0000803</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">Cysts of the cortex of 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">Renal cortical 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/869160" ref="tree=MeSH" title="MedGen record for Abnormal renal cortex morphology">Abnormal renal cortex morphology</a></span><ul><li><span class="matched_ds">Renal cortical cysts</span><ul><li><span class="TLline"><a href="/medgen/356391" ref="tree=MeSH" title="MedGen record for Renal cortical microcysts">Renal cortical microcysts</a></span></li></ul></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_2562"><div><strong>Beckwith-Wiedemann syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>2562</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.">C0004903</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by macroglossia, hemihyperplasia, omphalocele, neonatal hypoglycemia, macrosomia, embryonal tumors (e.g., Wilms tumor, hepatoblastoma, neuroblastoma, and rhabdomyosarcoma), visceromegaly, adrenocortical cytomegaly, kidney abnormalities (e.g., medullary dysplasia, nephrocalcinosis, and medullary sponge kidney), and ear creases / posterior helical ear pits. BWS is considered a clinical spectrum, in which affected individuals may have many or only one or two of the characteristic clinical features. Although most individuals with BWS show rapid growth in late fetal development and early childhood, growth rate usually slows by age seven to eight years. Adult heights are typically within the normal range. Hemihyperplasia (also known as lateralized overgrowth) is often appreciated at birth and may become more or less evident over time. Hemihyperplasia may affect segmental regions of the body or selected organs and tissues. Hemihyperplasia may be limited to one side of the body (ipsilateral) or involve opposite sides of the body (contralateral). Macroglossia is generally present at birth and can obstruct breathing or interfere with feeding in infants. Neonatal hypoglycemia occurs in approximately 50% of infants with BWS; most episodes are mild and transient. However, in some cases, persistent hypoglycemia due to hyperinsulinism may require consultation with an endocrinologist for therapeutic intervention. With respect to the increased risk for embryonal tumor development, the risk for Wilms tumor appears to be concentrated in the first seven years of life, whereas the risk for developing hepatoblastoma is concentrated in the first three to four years of life. Cognitive and neurobehavioral development is usually normal. After childhood, prognosis is generally favorable, although some adults experience issues requiring medical management (e.g., for renal or skeletal concerns).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/2562">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_75696"><div><strong>Multiple acyl-CoA dehydrogenase deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75696</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.">C0268596</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Multiple acyl-CoA dehydrogenase deficiency (MADD) represents a clinical spectrum in which presentations can be divided into type I (neonatal onset with congenital anomalies), type II (neonatal onset without congenital anomalies), and type III (late onset). Individuals with type I or II MADD typically become symptomatic in the neonatal period with severe metabolic acidosis, which may be accompanied by profound hypoglycemia and hyperammonemia. Many affected individuals die in the newborn period despite metabolic treatment. In those who survive the neonatal period, recurrent metabolic decompensation resembling Reye syndrome and the development of hypertrophic cardiomyopathy can occur. Congenital anomalies may include dysmorphic facial features, large cystic kidneys, hypospadias and chordee in males, and neuronal migration defects (heterotopias) on brain MRI. Individuals with type III MADD, the most common presentation, can present from infancy to adulthood. The most common symptoms are muscle weakness, exercise intolerance, and/or muscle pain, although metabolic decompensation with episodes of rhabdomyolysis can also be seen. Rarely, individuals with late-onset MADD (type III) may develop severe sensory neuropathy in addition to proximal myopathy.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75696">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_167105"><div><strong>C syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>167105</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.">C0796095</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The C syndrome, also known as Opitz trigonocephaly syndrome, is a malformation syndrome characterized by trigonocephaly, severe mental retardation, hypotonia, variable cardiac defects, redundant skin, and dysmorphic facial features, including upslanted palpebral fissures, epicanthal folds, depressed nasal bridge, and low-set, posteriorly rotated ears (summary by Kaname et al., 2007). C syndrome shows phenotypic overlap with Bohring-Opitz syndrome, or C-like syndrome (605039), a disorder with more severe features than C syndrome, caused by heterozygous mutation in the ASXL1 gene (612990) on chromosome 20q11.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/167105">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_322968"><div><strong>MPDU1-congenital disorder of glycosylation</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>322968</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.">C1836669</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Congenital disorders of glycosylation (CDGs) are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation. Different forms of CDGs can be recognized by altered isoelectric focusing (IEF) patterns of serum transferrin. For a discussion of the classification of CDGs, see CDG Ia (212065).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/322968">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_347545"><div><strong>Joubert syndrome 5</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347545</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.">C1857780</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Classic Joubert syndrome (JS) is characterized by three primary findings: A distinctive cerebellar and brain stem malformation called the molar tooth sign (MTS). Hypotonia. Developmental delays. Often these findings are accompanied by episodic tachypnea or apnea and/or atypical eye movements. In general, the breathing abnormalities improve with age, truncal ataxia develops over time, and acquisition of gross motor milestones is delayed. Cognitive abilities are variable, ranging from severe intellectual disability to normal. Additional findings can include retinal dystrophy, renal disease, ocular colobomas, occipital encephalocele, hepatic fibrosis, polydactyly, oral hamartomas, and endocrine abnormalities. Both intra- and interfamilial variation are seen.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/347545">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684735"><div><strong>Developmental and epileptic encephalopathy, 77</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684735</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.">C5231405</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Multiple congenital anomalies-hypotonia-seizures syndrome-4 (MCAHS4) is an autosomal recessive neurologic disorder characterized by onset of refractory seizures in the first months of life. Patients have severe global developmental delay, and may have additional variable features, including dysmorphic or coarse facial features, visual defects, and mild skeletal or renal anomalies. At the cellular level, the disorder is caused by a defect in the synthesis of glycosylphosphatidylinositol (GPI), and thus affects the expression of GPI-anchored proteins at the cell surface (summary by Starr et al., 2019). For a discussion of genetic heterogeneity of MCAHS, see MCAHS1 (614080). For a discussion of genetic heterogeneity of DEE, see 308350. For a discussion of genetic heterogeneity of GPI biosynthesis defects, see GPIBD1 (610293).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684735">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_2562" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Beckwith-Wiedemann syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_167105" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">C syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684735" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental and epileptic encephalopathy, 77</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_347545" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Joubert syndrome 5</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_322968" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">MPDU1-congenital disorder of glycosylation</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75696" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Multiple acyl-CoA dehydrogenase deficiency</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/39643905">Radiomics for differential diagnosis of Bosniak II-IV renal masses via CT imaging.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhao X,
|
||
Yan Y,
|
||
Xie W,
|
||
Qin Z,
|
||
Zhao L,
|
||
Liu C,
|
||
Zhang S,
|
||
Liu J,
|
||
Ma L</span><br />
|
||
<span class="medgenPMjournal">BMC Cancer</span>
|
||
2024 Dec 6;24(1):1508.
|
||
doi: 10.1186/s12885-024-13283-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39643905" target="_blank">39643905</a><a href="/pmc/articles/PMC11622457" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29181500">Perinatal Diagnosis, Management, and Follow-up of Cystic Renal Diseases: A Clinical Practice Recommendation With Systematic Literature Reviews.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gimpel C,
|
||
Avni FE,
|
||
Bergmann C,
|
||
Cetiner M,
|
||
Habbig S,
|
||
Haffner D,
|
||
König J,
|
||
Konrad M,
|
||
Liebau MC,
|
||
Pape L,
|
||
Rellensmann G,
|
||
Titieni A,
|
||
von Kaisenberg C,
|
||
Weber S,
|
||
Winyard PJD,
|
||
Schaefer F</span><br />
|
||
<span class="medgenPMjournal">JAMA Pediatr</span>
|
||
2018 Jan 1;172(1):74-86.
|
||
doi: 10.1001/jamapediatrics.2017.3938.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29181500" target="_blank">29181500</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=(renal%20cortical%20cysts)%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 (6)</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/31110385">Initial Experience of Retroperitoneoscopic Surgery in Benign Renal Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kunwar AK,
|
||
Upadhyay AM,
|
||
Shrestha SB,
|
||
Koirala U,
|
||
Tiwari K,
|
||
Dangal G</span><br />
|
||
<span class="medgenPMjournal">J Nepal Health Res Counc</span>
|
||
2019 Apr 28;17(1):94-99.
|
||
doi: 10.33314/jnhrc.1772.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31110385" target="_blank">31110385</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26375276">Antenatal Determinants of Long-Term Kidney Outcome in Boys with Posterior Urethral Valves.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsell DG,
|
||
Yu S,
|
||
Morrison SJ</span><br />
|
||
<span class="medgenPMjournal">Fetal Diagn Ther</span>
|
||
2016;39(3):214-21.
|
||
Epub 2015 Sep 17
|
||
doi: 10.1159/000439302.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26375276" target="_blank">26375276</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21301376">A prospective diagnostic accuracy study of F-18 fluorodeoxyglucose-positron emission tomography/computed tomography in the evaluation of indeterminate renal masses.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ozülker T,
|
||
Ozülker F,
|
||
Ozbek E,
|
||
Ozpaçaci T</span><br />
|
||
<span class="medgenPMjournal">Nucl Med Commun</span>
|
||
2011 Apr;32(4):265-72.
|
||
doi: 10.1097/MNM.0b013e3283442e3b.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21301376" target="_blank">21301376</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11433086">Fetal surgery for posterior urethral valves: long-term postnatal outcomes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Holmes N,
|
||
Harrison MR,
|
||
Baskin LS</span><br />
|
||
<span class="medgenPMjournal">Pediatrics</span>
|
||
2001 Jul;108(1):E7.
|
||
doi: 10.1542/peds.108.1.e7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11433086" target="_blank">11433086</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/841041">Some important radiological aspects of the kidney in Hippel-Lindau syndrome: the value of prospective study in an affected family.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee KR,
|
||
Wulfsberg E,
|
||
Kepes JJ</span><br />
|
||
<span class="medgenPMjournal">Radiology</span>
|
||
1977 Mar;122(3):649-53.
|
||
doi: 10.1148/122.3.649.
|
||
<span class="bold">PMID: </span><a href="/pubmed/841041" target="_blank">841041</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%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 (6)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28730376">Lower urinary tract obstruction: fetal intervention based on prenatal staging.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ruano R,
|
||
Dunn T,
|
||
Braun MC,
|
||
Angelo JR,
|
||
Safdar A</span><br />
|
||
<span class="medgenPMjournal">Pediatr Nephrol</span>
|
||
2017 Oct;32(10):1871-1878.
|
||
Epub 2017 Jul 21
|
||
doi: 10.1007/s00467-017-3593-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28730376" target="_blank">28730376</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26375276">Antenatal Determinants of Long-Term Kidney Outcome in Boys with Posterior Urethral Valves.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsell DG,
|
||
Yu S,
|
||
Morrison SJ</span><br />
|
||
<span class="medgenPMjournal">Fetal Diagn Ther</span>
|
||
2016;39(3):214-21.
|
||
Epub 2015 Sep 17
|
||
doi: 10.1159/000439302.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26375276" target="_blank">26375276</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7645145">Simple renal cortical cysts in children: two uncommon case reports.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Barzilai M</span><br />
|
||
<span class="medgenPMjournal">Urol Int</span>
|
||
1994;53(3):162-5.
|
||
doi: 10.1159/000282661.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7645145" target="_blank">7645145</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3550671">Computerized tomography and ultrasound in the diagnosis of cerebro-hepato-renal syndrome of Zellweger.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Weese-Mayer DE,
|
||
Smith KM,
|
||
Reddy JK,
|
||
Salafsky I,
|
||
Poznanski AK</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
1987;17(2):170-2.
|
||
doi: 10.1007/BF02388104.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3550671" target="_blank">3550671</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6729104">Fetal renal dysplasia: sonographic evaluation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mahony BS,
|
||
Filly RA,
|
||
Callen PW,
|
||
Hricak H,
|
||
Golbus MS,
|
||
Harrison MR</span><br />
|
||
<span class="medgenPMjournal">Radiology</span>
|
||
1984 Jul;152(1):143-6.
|
||
doi: 10.1148/radiology.152.1.6729104.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6729104" target="_blank">6729104</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%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 (17)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/19863205">A case of Jarcho-Levin syndrome associated with bilateral cystic renal disease and wilms tumor: MR imaging findings.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Inan N,
|
||
Corapcioglu F,
|
||
Akansel G,
|
||
Yildiz K,
|
||
Ozdamar AS,
|
||
Mutlu A</span><br />
|
||
<span class="medgenPMjournal">Pediatr Hematol Oncol</span>
|
||
2009 Oct-Nov;26(7):496-503.
|
||
doi: 10.1080/08880010902773263.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19863205" target="_blank">19863205</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3706414">Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wilson GN,
|
||
Holmes RG,
|
||
Custer J,
|
||
Lipkowitz JL,
|
||
Stover J,
|
||
Datta N,
|
||
Hajra A</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet</span>
|
||
1986 May;24(1):69-82.
|
||
doi: 10.1002/ajmg.1320240109.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3706414" target="_blank">3706414</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%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 (2)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29764427">COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Voskarides K,
|
||
Papagregoriou G,
|
||
Hadjipanagi D,
|
||
Petrou I,
|
||
Savva I,
|
||
Elia A,
|
||
Athanasiou Y,
|
||
Pastelli A,
|
||
Kkolou M,
|
||
Hadjigavriel M,
|
||
Stavrou C,
|
||
Pierides A,
|
||
Deltas C</span><br />
|
||
<span class="medgenPMjournal">BMC Nephrol</span>
|
||
2018 May 16;19(1):114.
|
||
doi: 10.1186/s12882-018-0906-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29764427" target="_blank">29764427</a><a href="/pmc/articles/PMC5954460" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28730376">Lower urinary tract obstruction: fetal intervention based on prenatal staging.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ruano R,
|
||
Dunn T,
|
||
Braun MC,
|
||
Angelo JR,
|
||
Safdar A</span><br />
|
||
<span class="medgenPMjournal">Pediatr Nephrol</span>
|
||
2017 Oct;32(10):1871-1878.
|
||
Epub 2017 Jul 21
|
||
doi: 10.1007/s00467-017-3593-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28730376" target="_blank">28730376</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26375276">Antenatal Determinants of Long-Term Kidney Outcome in Boys with Posterior Urethral Valves.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsell DG,
|
||
Yu S,
|
||
Morrison SJ</span><br />
|
||
<span class="medgenPMjournal">Fetal Diagn Ther</span>
|
||
2016;39(3):214-21.
|
||
Epub 2015 Sep 17
|
||
doi: 10.1159/000439302.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26375276" target="_blank">26375276</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11433086">Fetal surgery for posterior urethral valves: long-term postnatal outcomes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Holmes N,
|
||
Harrison MR,
|
||
Baskin LS</span><br />
|
||
<span class="medgenPMjournal">Pediatrics</span>
|
||
2001 Jul;108(1):E7.
|
||
doi: 10.1542/peds.108.1.e7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11433086" target="_blank">11433086</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6729104">Fetal renal dysplasia: sonographic evaluation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mahony BS,
|
||
Filly RA,
|
||
Callen PW,
|
||
Hricak H,
|
||
Golbus MS,
|
||
Harrison MR</span><br />
|
||
<span class="medgenPMjournal">Radiology</span>
|
||
1984 Jul;152(1):143-6.
|
||
doi: 10.1148/radiology.152.1.6729104.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6729104" target="_blank">6729104</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%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 (10)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31110385">Initial Experience of Retroperitoneoscopic Surgery in Benign Renal Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kunwar AK,
|
||
Upadhyay AM,
|
||
Shrestha SB,
|
||
Koirala U,
|
||
Tiwari K,
|
||
Dangal G</span><br />
|
||
<span class="medgenPMjournal">J Nepal Health Res Counc</span>
|
||
2019 Apr 28;17(1):94-99.
|
||
doi: 10.33314/jnhrc.1772.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31110385" target="_blank">31110385</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29764427">COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Voskarides K,
|
||
Papagregoriou G,
|
||
Hadjipanagi D,
|
||
Petrou I,
|
||
Savva I,
|
||
Elia A,
|
||
Athanasiou Y,
|
||
Pastelli A,
|
||
Kkolou M,
|
||
Hadjigavriel M,
|
||
Stavrou C,
|
||
Pierides A,
|
||
Deltas C</span><br />
|
||
<span class="medgenPMjournal">BMC Nephrol</span>
|
||
2018 May 16;19(1):114.
|
||
doi: 10.1186/s12882-018-0906-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29764427" target="_blank">29764427</a><a href="/pmc/articles/PMC5954460" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26375276">Antenatal Determinants of Long-Term Kidney Outcome in Boys with Posterior Urethral Valves.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsell DG,
|
||
Yu S,
|
||
Morrison SJ</span><br />
|
||
<span class="medgenPMjournal">Fetal Diagn Ther</span>
|
||
2016;39(3):214-21.
|
||
Epub 2015 Sep 17
|
||
doi: 10.1159/000439302.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26375276" target="_blank">26375276</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11433086">Fetal surgery for posterior urethral valves: long-term postnatal outcomes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Holmes N,
|
||
Harrison MR,
|
||
Baskin LS</span><br />
|
||
<span class="medgenPMjournal">Pediatrics</span>
|
||
2001 Jul;108(1):E7.
|
||
doi: 10.1542/peds.108.1.e7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11433086" target="_blank">11433086</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6729104">Fetal renal dysplasia: sonographic evaluation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mahony BS,
|
||
Filly RA,
|
||
Callen PW,
|
||
Hricak H,
|
||
Golbus MS,
|
||
Harrison MR</span><br />
|
||
<span class="medgenPMjournal">Radiology</span>
|
||
1984 Jul;152(1):143-6.
|
||
doi: 10.1148/radiology.152.1.6729104.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6729104" target="_blank">6729104</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Renal%20cortical%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 (8)</a></div></div>
|
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|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Renal%20cortical%20cysts" target="_blank">ClinicalTrials.gov</a></li></ul></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=(renal%20cortical%20cysts)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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