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<!--
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UID=326980
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ConceptID=C1839858
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Periventricular cysts</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>326980</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.">C1839858</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>HPO:</td>
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0007109">HP:0007109</a></td></tr>
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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">Periventricular cysts</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/871309" ref="tree=MeSH" title="MedGen record for Abnormality of prenatal development or birth">Abnormality of prenatal development or birth</a></span><ul><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/138106" ref="tree=MeSH" title="MedGen record for Central nervous system cyst">Central nervous system cyst</a></span><ul><li><span class="TLline"><a href="/medgen/866894" ref="tree=MeSH" title="MedGen record for Intracranial cystic lesion">Intracranial cystic lesion</a></span><ul><li><span class="matched_ds">Periventricular cysts</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="divPopper rprt" id="rdis_18145"><div><strong>Lowe syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>18145</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.">C0028860</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Lowe syndrome (oculocerebrorenal syndrome) is characterized by involvement of the eyes, central nervous system, and kidneys. Dense congenital cataracts are found in all affected boys and infantile glaucoma in approximately 50%. All boys have impaired vision; corrected acuity is rarely better than 20/100. Generalized hypotonia is noted at birth and is of central (brain) origin. Deep tendon reflexes are usually absent. Hypotonia may slowly improve with age, but normal motor tone and strength are never achieved. Motor milestones are delayed. Almost all affected males have some degree of intellectual disability; 10%-25% function in the low-normal or borderline range, approximately 25% in the mild-to-moderate range, and 50%-65% in the severe-to-profound range of intellectual disability. Affected males have varying degrees of proximal renal tubular dysfunction of the Fanconi type, including low molecular-weight (LMW) proteinuria, aminoaciduria, bicarbonate wasting and renal tubular acidosis, phosphaturia with hypophosphatemia and renal rickets, hypercalciuria, sodium and potassium wasting, and polyuria. The features of symptomatic Fanconi syndrome do not usually become manifest until after the first few months of life, except for LMW proteinuria. Glomerulosclerosis associated with chronic tubular injury usually results in slowly progressive chronic renal failure and end-stage renal disease between the second and fourth decades of life.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/18145">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_408255"><div><strong>4p partial monosomy syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>408255</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.">C1956097</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features ('Greek warrior helmet' appearance of the nose, high forehead, prominent glabella, hypertelorism, high-arched eyebrows, protruding eyes, epicanthal folds, short philtrum, distinct mouth with downturned corners, and micrognathia), and a seizure disorder (Battaglia et al., 2008).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/408255">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_815922"><div><strong>Mitochondrial DNA depletion syndrome 13</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>815922</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.">C3809592</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">FBXL4-related encephalomyopathic mitochondrial DNA (mtDNA) depletion syndrome is a multi-system disorder characterized primarily by congenital or early-onset lactic acidosis and growth failure, feeding difficulty, hypotonia, and developmental delay. Other neurologic manifestations can include seizures, movement disorders, ataxia, autonomic dysfunction, and stroke-like episodes. All affected individuals alive at the time they were reported (median age: 3.5 years) demonstrated significant developmental delay. Other findings can involve the heart (hypertrophic cardiomyopathy, congenital heart malformations, arrhythmias), liver (mildly elevated transaminases), eyes (cataract, strabismus, nystagmus, optic atrophy), hearing (sensorineural hearing loss), and bone marrow (neutropenia, lymphopenia). Survival varies; the median age of reported deaths was two years (range 2 days – 75 months), although surviving individuals as old as 36 years have been reported. To date FBXL4-related mtDNA depletion syndrome has been reported in 50 individuals.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/815922">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_863690"><div><strong>Mitochondrial complex III deficiency nuclear type 9</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>863690</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.">C4015253</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCC3 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/863690">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1380260"><div><strong>Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1380260</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.">C4479631</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies (NDMSBA) is an autosomal recessive neurodevelopmental disorder characterized by infantile onset of progressive microcephaly and spasticity and severe global developmental delay resulting in profoundly impaired intellectual development and severely impaired or absent motor function. More variable features include seizures and optic atrophy. Brain imaging may show myelinating abnormalities and white matter lesions consistent with a leukoencephalopathy, as well as structural anomalies, including thin corpus callosum, gyral abnormalities, and cerebral or cerebellar atrophy. Some patients die in early childhood (summary by Falik Zaccai et al., 2017 and Hall et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1380260">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1624694"><div><strong>Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1624694</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.">C4540052</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">NELABA is a severe autosomal recessive metabolic disorder characterized by onset at birth of progressive encephalopathy associated with increased serum lactate. Affected individuals have little or no psychomotor development and show brain abnormalities, including cerebral atrophy, cysts, and white matter abnormalities. Some patients die in infancy (summary by Habarou et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1624694">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1770895"><div><strong>Rajab interstitial lung disease with brain calcifications 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1770895</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.">C5436603</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Rajab interstitial lung disease with brain calcifications-2 (RILDBC2) is an autosomal recessive disorder characterized by growth delay, interstitial lung disease, liver disease, and abnormal brain MRI findings, including brain calcifications and periventricular cysts (Krenke et al., 2019). For a discussion of genetic heterogeneity of RILDBC, see RILDBC1 (613658).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1770895">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1775930"><div><strong>Neurodevelopmental disorder with alopecia and brain abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1775930</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.">C5436741</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Bachmann-Bupp syndrome (BABS) is characterized by a distinctive type of alopecia, global developmental delay in the moderate to severe range, hypotonia, nonspecific dysmorphic features, behavioral abnormalities (autism spectrum disorder, attention-deficit/hyperactivity disorder) and feeding difficulties. Hair is typically present at birth but may be sparse and of an unexpected color with subsequent loss of hair in large clumps within the first few weeks of life. Rare findings may include seizures with onset in later childhood and conductive hearing loss.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1775930">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1841145"><div><strong>Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1841145</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.">C5830509</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity (NEDIHSS) is an autosomal recessive disorder characterized by prenatal or neonatal onset of intracranial hemorrhage, usually with ventriculomegaly and calcifications, resulting in parenchymal brain damage. Some affected individuals have symptoms incompatible with life and die in utero. Those that survive show profound global developmental delay with almost no motor or cognitive skills, hypotonia, spasticity, and seizures. Other features may include facial dysmorphism, retinal vascular abnormalities, and poor overall growth. The pathogenesis of the disease likely results from dysfunction of vascular endothelial cells in the brain (Lecca et al., 2023).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1841145">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_408255" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">4p partial monosomy syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1624694" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_18145" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lowe syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_863690" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mitochondrial complex III deficiency nuclear type 9</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_815922" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mitochondrial DNA depletion syndrome 13</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (9)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1775930" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with alopecia and brain abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1841145" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1380260" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1770895" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Rajab interstitial lung disease with brain calcifications 2</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33214065">Cranial ultrasonographic screening findings among healthy neonates and their association with neurodevelopmental outcomes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lin YJ,
|
||
Chiu NC,
|
||
Chen HJ,
|
||
Huang JY,
|
||
Ho CS</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neonatol</span>
|
||
2021 Mar;62(2):158-164.
|
||
Epub 2020 Nov 2
|
||
doi: 10.1016/j.pedneo.2020.10.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33214065" target="_blank">33214065</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27609618">Prenatal Evaluation, Imaging Features, and Neurodevelopmental Outcome of Prenatally Diagnosed Periventricular Pseudocysts.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cooper S,
|
||
Bar-Yosef O,
|
||
Berkenstadt M,
|
||
Hoffmann C,
|
||
Achiron R,
|
||
Katorza E</span><br />
|
||
<span class="medgenPMjournal">AJNR Am J Neuroradiol</span>
|
||
2016 Dec;37(12):2382-2388.
|
||
Epub 2016 Sep 8
|
||
doi: 10.3174/ajnr.A4916.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27609618" target="_blank">27609618</a><a href="/pmc/articles/PMC7963870" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12879343">Dandy-Walker malformation: prenatal diagnosis and prognosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Klein O,
|
||
Pierre-Kahn A,
|
||
Boddaert N,
|
||
Parisot D,
|
||
Brunelle F</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2003 Aug;19(7-8):484-9.
|
||
Epub 2003 Jul 16
|
||
doi: 10.1007/s00381-003-0782-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12879343" target="_blank">12879343</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(periventricular%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 (8)</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/37059118">Obliterated cavum septi pellucidi: Clinical significance and role of fetal magnetic resonance.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fantasia I,
|
||
Ciardo C,
|
||
Bracalente G,
|
||
Filippi E,
|
||
Murru FM,
|
||
Spezzacatene A,
|
||
Bin M,
|
||
Mendez Quintero O,
|
||
Montaguti E,
|
||
Lees C,
|
||
Papanikolaou K,
|
||
Pilu G,
|
||
Prefumo F,
|
||
Thilaganathan B,
|
||
Stampalija T</span><br />
|
||
<span class="medgenPMjournal">Acta Obstet Gynecol Scand</span>
|
||
2023 Jun;102(6):744-750.
|
||
Epub 2023 Apr 14
|
||
doi: 10.1111/aogs.14575.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37059118" target="_blank">37059118</a><a href="/pmc/articles/PMC10201966" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32437297">Clinical profile of symptomatic congenital cytomegalovirus infection: cases from a tertiary hospital in north India.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bhattacharya D,
|
||
Panigrahi I,
|
||
Chaudhry C</span><br />
|
||
<span class="medgenPMjournal">Trop Doct</span>
|
||
2020 Jul;50(3):282-284.
|
||
Epub 2020 May 21
|
||
doi: 10.1177/0049475520923491.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32437297" target="_blank">32437297</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17607600">Brain magnetic resonance imaging in Wolf-Hirschhorn syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Righini A,
|
||
Ciosci R,
|
||
Selicorni A,
|
||
Bianchini E,
|
||
Parazzini C,
|
||
Zollino M,
|
||
Lodi M,
|
||
Triulzi F</span><br />
|
||
<span class="medgenPMjournal">Neuropediatrics</span>
|
||
2007 Feb;38(1):25-8.
|
||
doi: 10.1055/s-2007-981685.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17607600" target="_blank">17607600</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8046042">Neurosonographic findings in full-term infants born to maternal cocaine abusers: visualization of subependymal and periventricular cysts.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cohen HL,
|
||
Sloves JH,
|
||
Laungani S,
|
||
Glass L,
|
||
DeMarinis P</span><br />
|
||
<span class="medgenPMjournal">J Clin Ultrasound</span>
|
||
1994 Jun;22(5):327-33.
|
||
doi: 10.1002/jcu.1870220507.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8046042" target="_blank">8046042</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7684121">The high-risk infant.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Allen MC</span><br />
|
||
<span class="medgenPMjournal">Pediatr Clin North Am</span>
|
||
1993 Jun;40(3):479-90.
|
||
doi: 10.1016/s0031-3955(16)38545-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7684121" target="_blank">7684121</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periventricular%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 (32)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32437297">Clinical profile of symptomatic congenital cytomegalovirus infection: cases from a tertiary hospital in north India.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bhattacharya D,
|
||
Panigrahi I,
|
||
Chaudhry C</span><br />
|
||
<span class="medgenPMjournal">Trop Doct</span>
|
||
2020 Jul;50(3):282-284.
|
||
Epub 2020 May 21
|
||
doi: 10.1177/0049475520923491.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32437297" target="_blank">32437297</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25647544">Leukodystrophy with multiple beaded periventricular cysts: unusual cranial MRI results in Canavan disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Drenckhahn A,
|
||
Schuelke M,
|
||
Knierim E</span><br />
|
||
<span class="medgenPMjournal">J Inherit Metab Dis</span>
|
||
2015 Sep;38(5):983-4.
|
||
Epub 2015 Feb 3
|
||
doi: 10.1007/s10545-015-9812-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25647544" target="_blank">25647544</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20823030">Experience with hyperphenylalaninemia in a developing country: unusual clinical manifestations and a novel gene mutation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Karam PE,
|
||
Daher RT,
|
||
Moller LB,
|
||
Mikati MA</span><br />
|
||
<span class="medgenPMjournal">J Child Neurol</span>
|
||
2011 Feb;26(2):142-6.
|
||
Epub 2010 Sep 7
|
||
doi: 10.1177/0883073810375116.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20823030" target="_blank">20823030</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9613526">The Proteus syndrome: CNS manifestations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dietrich RB,
|
||
Glidden DE,
|
||
Roth GM,
|
||
Martin RA,
|
||
Demo DS</span><br />
|
||
<span class="medgenPMjournal">AJNR Am J Neuroradiol</span>
|
||
1998 May;19(5):987-90.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9613526" target="_blank">9613526</a><a href="/pmc/articles/PMC8337570" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7684121">The high-risk infant.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Allen MC</span><br />
|
||
<span class="medgenPMjournal">Pediatr Clin North Am</span>
|
||
1993 Jun;40(3):479-90.
|
||
doi: 10.1016/s0031-3955(16)38545-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7684121" target="_blank">7684121</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periventricular%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 (42)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30549340">Role of magnetic resonance imaging in fetuses with mild or moderate ventriculomegaly in the era of fetal neurosonography: systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Di Mascio D,
|
||
Sileo FG,
|
||
Khalil A,
|
||
Rizzo G,
|
||
Persico N,
|
||
Brunelli R,
|
||
Giancotti A,
|
||
Panici PB,
|
||
Acharya G,
|
||
D'Antonio F</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
|
||
2019 Aug;54(2):164-171.
|
||
Epub 2019 Jul 11
|
||
doi: 10.1002/uog.20197.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30549340" target="_blank">30549340</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25432856">Surgical management of complex multiloculated hydrocephalus in infants and children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Akbari SH,
|
||
Holekamp TF,
|
||
Murphy TM,
|
||
Mercer D,
|
||
Leonard JR,
|
||
Smyth MD,
|
||
Park TS,
|
||
Limbrick DD Jr</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2015 Feb;31(2):243-9.
|
||
Epub 2014 Nov 29
|
||
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<div class="portlet_content ln"><span class="medgenPMauthor">Taylor GA,
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<div class="nl"><a target="_blank" href="/pubmed/37122081">Vestibular Follow-up Program for Congenital Cytomegalovirus Based on 6 Years of Longitudinal Data Collection.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Dhondt C,
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Maes L,
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Van Acker E,
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Martens S,
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Rombaut L,
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De Cuyper E,
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Van Hoecke H,
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De Leenheer E,
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Epub 2023 May 1
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<span class="bold">PMID: </span><a href="/pubmed/37122081" target="_blank">37122081</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/36054219">Predicting Early Vestibular and Motor Function in Congenital Cytomegalovirus Infection.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Dhondt C,
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Maes L,
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Martens S,
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Vanaudenaerde S,
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Rombaut L,
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Sucaet M,
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Keymeulen A,
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Epub 2022 Sep 2
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<span class="bold">PMID: </span><a href="/pubmed/36054219" target="_blank">36054219</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34531153">Association between neuroimaging findings and neurological sequelae in patients with congenital cytomegalovirus infection.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Escobar Castellanos M,
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de la Mata Navazo S,
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Carrón Bermejo M,
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García Morín M,
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Ruiz Martín Y,
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Saavedra Lozano J,
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Miranda Herrero MC,
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Barredo Valderrama E,
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Castro de Castro P,
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Vázquez López M</span><br />
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Epub 2021 Sep 14
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<span class="bold">PMID: </span><a href="/pubmed/34531153" target="_blank">34531153</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/25663021">MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Baertling F,
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Haack TB,
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Rodenburg RJ,
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Schaper J,
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Seibt A,
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Strom TM,
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Meitinger T,
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Mayatepek E,
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<span class="bold">PMID: </span><a href="/pubmed/25663021" target="_blank">25663021</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/16151915">Fumarase deficiency presenting with periventricular cysts.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Loeffen J,
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Voit T,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periventricular%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 (24)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36580312">Risk Factors for Hearing Loss at Birth in Newborns With Congenital Cytomegalovirus Infection.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">De Cuyper E,
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Acke F,
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Keymeulen A,
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De Leenheer EMR,
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Van Hoecke H,
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Padalko E,
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Boudewyns A,
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Gilles A,
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Muylle M,
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Kuhweide R,
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Royackers L,
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Desloovere C,
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Verstreken M,
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Schatteman I,
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Dhooge I</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/36580312" target="_blank">36580312</a><a href="/pmc/articles/PMC9857716" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36054219">Predicting Early Vestibular and Motor Function in Congenital Cytomegalovirus Infection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dhondt C,
|
||
Maes L,
|
||
Martens S,
|
||
Vanaudenaerde S,
|
||
Rombaut L,
|
||
Sucaet M,
|
||
Keymeulen A,
|
||
Van Hoecke H,
|
||
De Leenheer E,
|
||
Dhooge I</span><br />
|
||
<span class="medgenPMjournal">Laryngoscope</span>
|
||
2023 Jul;133(7):1757-1765.
|
||
Epub 2022 Sep 2
|
||
doi: 10.1002/lary.30375.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36054219" target="_blank">36054219</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34531153">Association between neuroimaging findings and neurological sequelae in patients with congenital cytomegalovirus infection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Escobar Castellanos M,
|
||
de la Mata Navazo S,
|
||
Carrón Bermejo M,
|
||
García Morín M,
|
||
Ruiz Martín Y,
|
||
Saavedra Lozano J,
|
||
Miranda Herrero MC,
|
||
Barredo Valderrama E,
|
||
Castro de Castro P,
|
||
Vázquez López M</span><br />
|
||
<span class="medgenPMjournal">Neurologia (Engl Ed)</span>
|
||
2022 Mar;37(2):122-129.
|
||
Epub 2021 Sep 14
|
||
doi: 10.1016/j.nrleng.2018.11.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34531153" target="_blank">34531153</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30549340">Role of magnetic resonance imaging in fetuses with mild or moderate ventriculomegaly in the era of fetal neurosonography: systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Di Mascio D,
|
||
Sileo FG,
|
||
Khalil A,
|
||
Rizzo G,
|
||
Persico N,
|
||
Brunelli R,
|
||
Giancotti A,
|
||
Panici PB,
|
||
Acharya G,
|
||
D'Antonio F</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
|
||
2019 Aug;54(2):164-171.
|
||
Epub 2019 Jul 11
|
||
doi: 10.1002/uog.20197.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30549340" target="_blank">30549340</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18991326">Prenatal ultrasonographic diagnosis of polymicrogyria.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dhombres F,
|
||
Nahama-Allouche C,
|
||
Gelot A,
|
||
Jouannic JM,
|
||
de Villemeur TB,
|
||
Saint-Frison MH,
|
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le Pointe HD,
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Garel C</span><br />
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<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
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2008 Dec;32(7):951-4.
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doi: 10.1002/uog.6251.
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<span class="bold">PMID: </span><a href="/pubmed/18991326" target="_blank">18991326</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periventricular%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 (18)</a></div></div>
|
||
</div>
|
||
|
||
<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>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/30549340">Role of magnetic resonance imaging in fetuses with mild or moderate ventriculomegaly in the era of fetal neurosonography: systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Di Mascio D,
|
||
Sileo FG,
|
||
Khalil A,
|
||
Rizzo G,
|
||
Persico N,
|
||
Brunelli R,
|
||
Giancotti A,
|
||
Panici PB,
|
||
Acharya G,
|
||
D'Antonio F</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
|
||
2019 Aug;54(2):164-171.
|
||
Epub 2019 Jul 11
|
||
doi: 10.1002/uog.20197.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30549340" target="_blank">30549340</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Periventricular%20cysts%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 (1)</a></div></div>
|
||
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|
||
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|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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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=(periventricular%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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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Periventricular%20cysts" target="_blank">MedlinePlus</a></li></ul></div>
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<a href="/pubmed/clinical?term=Periventricular%20cysts" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Periventricular%20cysts%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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<a href="https://www.google.com/maps/place/8600+Rockville+Pike,+Bethesda,+MD+20894/@38.9959508,-77.101021,17z/data=!3m1!4b1!4m5!3m4!1s0x89b7c95e25765ddb:0x19156f88b27635b8!8m2!3d38.9959508!4d-77.0988323" class="text-white" target="_blank" rel="noopener noreferrer">8600 Rockville Pike<br />
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Bethesda, MD 20894</a></p>
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<p><a href="https://www.nlm.nih.gov/web_policies.html" class="text-white">Web Policies</a><br />
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