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<meta name="keywords" content="C0026654, cerebrovascular moyamoya disease, disease or syndrome, disease, moya-moya, idiopathic moyamoya disease, moya moya disease, moya-moya disease, moyamoya, moyamoya disease, moyamoya disease, primary, moyamoya disease, secondary, moyamoya syndrome, mymy, progressive intracranial arterial occlusion, progressive intracranial occlusive arteropathy (moyamoya), autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="Moyamoya is the name given to a cerebral angiographic picture of bilateral intracranial carotid artery occlusion associated with telangiectatic vessels in the region of the basal ganglia. The Japanese word moyamoya means 'something hazy like a puff of cigarette smoke, drifting in the air.' Hemiplegia of sudden onset and epileptic seizures constitute the prevailing presentation in childhood, while subarachnoid bleeding occurs more frequently in adults (summary by Suzuki, 1986). Genetic Heterogeneity of Moyamoya Disease The MYMY1 locus maps to chromosome 3p. See also susceptibility to moyamoya disease-2 (MYMY2; 607151), caused by variation in the RNF213 gene (613768) on chromosome 17q25; MYMY3 (608796), which maps to chromosome 8q23; MYMY5 (614042), caused by mutation in the ACTA2 gene (102620) on chromosome 10q23; MYMY6 with achalasia (615750), caused by mutation in the GUCY1A3 gene (139396) on chromosome 4q32; and MYMY7 (620687), caused by mutation in the ANO1 gene (610108) on chromosome 11q13. See also MYMY4 (300845), an X-linked recessive syndromic disorder characterized by moyamoya disease, short stature, hypergonadotropic hypogonadism, and facial dysmorphism." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=7726
|
||
ConceptID=C0026654
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Moyamoya disease</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>7726</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C0026654</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Moyamoya syndrome</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Moyamoya disease (69116000); Progressive intracranial arterial occlusion (89142007)</td></tr>
|
||
<tr><td>Modes of inheritance:</td>
|
||
<td>
|
||
<div class="divPopper rprt" id="moi_141025"><div><strong>Autosomal recessive inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141025</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.">C0441748</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Intellectual Product</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).</div></div>
|
||
<div class="divPopper rprt" id="moi_141047"><div><strong>Autosomal dominant inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141047</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.">C0443147</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Intellectual Product</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.</div></div>
|
||
<div class="divPopper rprt" id="moi_109109"><div><strong>Non-Mendelian inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>109109</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.">C0600599</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Genetic Function</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that depends on genetic determinants in more than one gene.</div></div>
|
||
<div class="divPopper rprt" id="moi_375779"><div><strong>X-linked recessive inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>375779</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.">C1845977</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for recessive traits related to a gene encoded on the X chromosome. In the context of medical genetics, X-linked recessive disorders manifest in males (who have one copy of the X chromosome and are thus hemizygotes), but generally not in female heterozygotes who have one mutant and one normal allele.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/375779">This record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_141025" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive inheritance</a><span> (Orphanet)</span></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_141047" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant inheritance</a><span> (Orphanet)</span></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_109109" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Non-Mendelian inheritance</a><span> (Orphanet)</span></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_375779" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">X-linked recessive inheritance</a><span> (Orphanet)</span></div></td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0016820" target="_blank">MONDO:0016820</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span> Phenotypic series:</td>
|
||
<td><a href="https://omim.org/phenotypicSeries/PS252350" target="_blank">PS252350</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=2573">ORPHA2573</a></td></tr></tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
|
||
<div class="portlet mgSection" id="ID_100">
|
||
<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">Moyamoya is the name given to a cerebral angiographic picture of bilateral intracranial carotid artery occlusion associated with telangiectatic vessels in the region of the basal ganglia. The Japanese word moyamoya means 'something hazy like a puff of cigarette smoke, drifting in the air.' Hemiplegia of sudden onset and epileptic seizures constitute the prevailing presentation in childhood, while subarachnoid bleeding occurs more frequently in adults (summary by Suzuki, 1986). Genetic Heterogeneity of Moyamoya Disease The MYMY1 locus maps to chromosome 3p. See also susceptibility to moyamoya disease-2 (MYMY2; 607151), caused by variation in the RNF213 gene (613768) on chromosome 17q25; MYMY3 (608796), which maps to chromosome 8q23; MYMY5 (614042), caused by mutation in the ACTA2 gene (102620) on chromosome 10q23; MYMY6 with achalasia (615750), caused by mutation in the GUCY1A3 gene (139396) on chromosome 4q32; and MYMY7 (620687), caused by mutation in the ANO1 gene (610108) on chromosome 11q13. See also MYMY4 (300845), an X-linked recessive syndromic disorder characterized by moyamoya disease, short stature, hypergonadotropic hypogonadism, and facial dysmorphism. [from <a title="Online Mendelian Inheritance in Man" href="http://www.omim.org" class="defSource" target="_blank">OMIM</a>]</div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_117">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Additional_description">Additional description</h1><a sid="117" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><div class="mgSection"><strong>From MedlinePlus Genetics</strong><br />Moyamoya disease is a disorder of blood vessels in the brain, specifically the internal carotid arteries and the arteries that branch from them. These vessels, which provide oxygen-rich blood to the brain, narrow over time. Narrowing of these vessels reduces blood flow in the brain. In an attempt to compensate, new networks of small, fragile blood vessels form. These networks, visualized by a particular test called an angiogram, resemble puffs of smoke, which is how the condition got its name: "moyamoya" is an expression meaning "something hazy like a puff of smoke" in Japanese.<br /><br />Some people have the blood vessel changes characteristic of moyamoya disease in addition to features of another disorder, such as neurofibromatosis type 1, sickle cell disease, or Graves' disease. These individuals are said to have moyamoya syndrome.<br /><br />Moyamoya disease commonly begins either around age 5 or in a person's thirties or forties. A lack of blood supply to the brain leads to several symptoms of the disorder, including temporary stroke-like episodes (transient ischemic attacks), strokes, and seizures. In addition, the fragile blood vessels that grow can develop bulges (aneurysms), or they can break open, leading to bleeding (hemorrhage) in the brain. Affected individuals may develop recurrent headaches, involuntary jerking movements (chorea), or a decline in thinking ability. The symptoms of moyamoya disease often worsen over time if the condition is not treated. <a target="_blank" href="https://medlineplus.gov/genetics/condition/moyamoya-disease">https://medlineplus.gov/genetics/condition/moyamoya-disease</a></div></div>
|
||
</div>
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|
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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>
|
||
<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="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0026654[DISCUI]&test_type=Clinical" ref="ncbi_uid=7726">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=7726" ref="ncbi_uid=7726">V</a></span></span><span class="TLline">Moyamoya disease</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/18325" ref="tree=MeSH" title="MedGen record for Pathological process">Pathological process</a></span><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/232130" ref="tree=MeSH" title="MedGen record for Disorder by Site">Disorder by Site</a></span><ul><li><span class="TLline"><a href="/medgen/2848" ref="tree=MeSH" title="MedGen record for Disorder of cardiovascular system">Disorder of cardiovascular system</a></span><ul><li><span class="TLline"><a href="/medgen/22621" ref="tree=MeSH" title="MedGen record for Vascular disorder">Vascular disorder</a></span><ul><li><span class="TLline"><a href="/medgen/13913" ref="tree=MeSH" title="MedGen record for Arterial occlusive disease">Arterial occlusive disease</a></span><ul><li><span class="matched_ds">Moyamoya disease</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_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/35197402">2021 Japanese Guidelines for the Management of Moyamoya Disease: Guidelines from the Research Committee on Moyamoya Disease and Japan Stroke Society.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fujimura M,
|
||
Tominaga T,
|
||
Kuroda S,
|
||
Takahashi JC,
|
||
Endo H,
|
||
Ogasawara K,
|
||
Miyamoto S;
|
||
Research Committee on Moyamoya Disease (Spontaneous Occlusion of Circle of Willis) of the Ministry of Health, Labor Welfare, Japan;
|
||
Guideline Committee 2021 of the Japan Stroke Society</span><br />
|
||
<span class="medgenPMjournal">Neurol Med Chir (Tokyo)</span>
|
||
2022 Apr 15;62(4):165-170.
|
||
Epub 2022 Feb 22
|
||
doi: 10.2176/jns-nmc.2021-0382.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35197402" target="_blank">35197402</a><a href="/pmc/articles/PMC9093674" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34279201">Progression in Moyamoya Disease: Clinical Features, Neuroimaging Evaluation, and Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang X,
|
||
Xiao W,
|
||
Zhang Q,
|
||
Xia D,
|
||
Gao P,
|
||
Su J,
|
||
Yang H,
|
||
Gao X,
|
||
Ni W,
|
||
Lei Y,
|
||
Gu Y</span><br />
|
||
<span class="medgenPMjournal">Curr Neuropharmacol</span>
|
||
2022;20(2):292-308.
|
||
doi: 10.2174/1570159X19666210716114016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34279201" target="_blank">34279201</a><a href="/pmc/articles/PMC9413783" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29343587">Surgical Management of Moyamoya Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Acker G,
|
||
Fekonja L,
|
||
Vajkoczy P</span><br />
|
||
<span class="medgenPMjournal">Stroke</span>
|
||
2018 Feb;49(2):476-482.
|
||
Epub 2018 Jan 17
|
||
doi: 10.1161/STROKEAHA.117.018563.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29343587" target="_blank">29343587</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22moyamoya%20disease%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 (108)</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/37609846">Adult Moyamoya Disease and Syndrome: Current Perspectives and Future Directions: A Scientific Statement From the American Heart Association/American Stroke Association.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gonzalez NR,
|
||
Amin-Hanjani S,
|
||
Bang OY,
|
||
Coffey C,
|
||
Du R,
|
||
Fierstra J,
|
||
Fraser JF,
|
||
Kuroda S,
|
||
Tietjen GE,
|
||
Yaghi S;
|
||
American Heart Association Stroke Council; Council on Cardiovascular and Stroke Nursing; and Council on Clinical Cardiology</span><br />
|
||
<span class="medgenPMjournal">Stroke</span>
|
||
2023 Oct;54(10):e465-e479.
|
||
Epub 2023 Aug 23
|
||
doi: 10.1161/STR.0000000000000443.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37609846" target="_blank">37609846</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35605621">Moyamoya disease: diagnosis and interventions.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ihara M,
|
||
Yamamoto Y,
|
||
Hattori Y,
|
||
Liu W,
|
||
Kobayashi H,
|
||
Ishiyama H,
|
||
Yoshimoto T,
|
||
Miyawaki S,
|
||
Clausen T,
|
||
Bang OY,
|
||
Steinberg GK,
|
||
Tournier-Lasserve E,
|
||
Koizumi A</span><br />
|
||
<span class="medgenPMjournal">Lancet Neurol</span>
|
||
2022 Aug;21(8):747-758.
|
||
Epub 2022 May 20
|
||
doi: 10.1016/S1474-4422(22)00165-X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35605621" target="_blank">35605621</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33563374">Intracranial Vascular Procedures.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gross WL,
|
||
Sacho RH</span><br />
|
||
<span class="medgenPMjournal">Anesthesiol Clin</span>
|
||
2021 Mar;39(1):1-18.
|
||
Epub 2021 Jan 9
|
||
doi: 10.1016/j.anclin.2020.10.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33563374" target="_blank">33563374</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29343587">Surgical Management of Moyamoya Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Acker G,
|
||
Fekonja L,
|
||
Vajkoczy P</span><br />
|
||
<span class="medgenPMjournal">Stroke</span>
|
||
2018 Feb;49(2):476-482.
|
||
Epub 2018 Jan 17
|
||
doi: 10.1161/STROKEAHA.117.018563.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29343587" target="_blank">29343587</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1781186">Moyamoya disease in Korea.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yu GJ,
|
||
Kim SY,
|
||
Coe CJ</span><br />
|
||
<span class="medgenPMjournal">Yonsei Med J</span>
|
||
1991 Sep;32(3):263-9.
|
||
doi: 10.3349/ymj.1991.32.3.263.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1781186" target="_blank">1781186</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Moyamoya%20disease%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 (1881)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36115805">Moyamoya disease emerging as an immune-related angiopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Asselman C,
|
||
Hemelsoet D,
|
||
Eggermont D,
|
||
Dermaut B,
|
||
Impens F</span><br />
|
||
<span class="medgenPMjournal">Trends Mol Med</span>
|
||
2022 Nov;28(11):939-950.
|
||
Epub 2022 Sep 14
|
||
doi: 10.1016/j.molmed.2022.08.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36115805" target="_blank">36115805</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35605621">Moyamoya disease: diagnosis and interventions.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ihara M,
|
||
Yamamoto Y,
|
||
Hattori Y,
|
||
Liu W,
|
||
Kobayashi H,
|
||
Ishiyama H,
|
||
Yoshimoto T,
|
||
Miyawaki S,
|
||
Clausen T,
|
||
Bang OY,
|
||
Steinberg GK,
|
||
Tournier-Lasserve E,
|
||
Koizumi A</span><br />
|
||
<span class="medgenPMjournal">Lancet Neurol</span>
|
||
2022 Aug;21(8):747-758.
|
||
Epub 2022 May 20
|
||
doi: 10.1016/S1474-4422(22)00165-X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35605621" target="_blank">35605621</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30455272">Moyamoya disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kondo T</span><br />
|
||
<span class="medgenPMjournal">CMAJ</span>
|
||
2018 Nov 19;190(46):E1364.
|
||
doi: 10.1503/cmaj.180681.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30455272" target="_blank">30455272</a><a href="/pmc/articles/PMC6239913" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19297575">Moyamoya disease and moyamoya syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Scott RM,
|
||
Smith ER</span><br />
|
||
<span class="medgenPMjournal">N Engl J Med</span>
|
||
2009 Mar 19;360(12):1226-37.
|
||
doi: 10.1056/NEJMra0804622.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19297575" target="_blank">19297575</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6759271">Moyamoya disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Levin S</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
1982 Dec;24(6):850-3.
|
||
doi: 10.1111/j.1469-8749.1982.tb13707.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6759271" target="_blank">6759271</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Moyamoya%20disease%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 (1708)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38913594">Exploration of the risk factor for infarction after revascularization in moyamoya disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sun T,
|
||
Zeng Q,
|
||
Huang L,
|
||
Sun J,
|
||
Wu Z,
|
||
Zhang B,
|
||
Ling C,
|
||
Chen C,
|
||
Wang H</span><br />
|
||
<span class="medgenPMjournal">Ann Med</span>
|
||
2024 Dec;56(1):2362872.
|
||
Epub 2024 Jun 24
|
||
doi: 10.1080/07853890.2024.2362872.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38913594" target="_blank">38913594</a><a href="/pmc/articles/PMC11198149" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28240586">Moyamoya disease and systemic sclerosis (MoSys syndrome): a combination of two rare entities: comment to the authors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">De Langhe E,
|
||
Lenaerts J,
|
||
Demaerel P,
|
||
Lemmens R</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Rheumatol</span>
|
||
2017 Sep-Oct;35 Suppl 106(4):216.
|
||
Epub 2017 Feb 23
|
||
<span class="bold">PMID: </span><a href="/pubmed/28240586" target="_blank">28240586</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27960175">Moyamoya Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fujimura M,
|
||
Bang OY,
|
||
Kim JS</span><br />
|
||
<span class="medgenPMjournal">Front Neurol Neurosci</span>
|
||
2016;40:204-220.
|
||
Epub 2016 Dec 2
|
||
doi: 10.1159/000448314.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27960175" target="_blank">27960175</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24814523">Anesthesia for interventional radiology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Landrigan-Ossar M,
|
||
McClain CD</span><br />
|
||
<span class="medgenPMjournal">Paediatr Anaesth</span>
|
||
2014 Jul;24(7):698-702.
|
||
Epub 2014 May 12
|
||
doi: 10.1111/pan.12411.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24814523" target="_blank">24814523</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7485948">Anaesthesia and moyamoya disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Henderson MA,
|
||
Irwin MG</span><br />
|
||
<span class="medgenPMjournal">Anaesth Intensive Care</span>
|
||
1995 Aug;23(4):503-6.
|
||
doi: 10.1177/0310057X9502300419.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7485948" target="_blank">7485948</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Moyamoya%20disease%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 (658)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29343587">Surgical Management of Moyamoya Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Acker G,
|
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Fekonja L,
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Vajkoczy P</span><br />
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2018 Feb;49(2):476-482.
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doi: 10.1161/STROKEAHA.117.018563.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29343587" target="_blank">29343587</a></div>
|
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<div class="nl"><a target="_blank" href="/pubmed/27637962">Cerebrovascular disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Portegies ML,
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2016;138:239-61.
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<span class="bold">PMID: </span><a href="/pubmed/27637962" target="_blank">27637962</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/27549666">Moyamoya Disease: A Review of Clinical Research.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Hishikawa T,
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<span class="bold">PMID: </span><a href="/pubmed/27549666" target="_blank">27549666</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/12760172">Moyamoya disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Yonekawa Y,
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2003;92:113-8.
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<span class="bold">PMID: </span><a href="/pubmed/12760172" target="_blank">12760172</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/2646161">Childhood moyamoya disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gordon N,
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<span class="medgenPMjournal">Dev Med Child Neurol</span>
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<span class="bold">PMID: </span><a href="/pubmed/2646161" target="_blank">2646161</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Moyamoya%20disease%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 (1071)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39043157">Adult Moyamoya Disease and Moyamoya Syndrome: What Is New?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Uchiyama S,
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Fujimura M</span><br />
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<span class="medgenPMjournal">Cerebrovasc Dis Extra</span>
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||
2024;14(1):86-94.
|
||
Epub 2024 Jul 23
|
||
doi: 10.1159/000540254.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39043157" target="_blank">39043157</a><a href="/pmc/articles/PMC11521421" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33567654">Pathological Circulating Factors in Moyamoya Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fang YC,
|
||
Wei LF,
|
||
Hu CJ,
|
||
Tu YK</span><br />
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<span class="medgenPMjournal">Int J Mol Sci</span>
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||
2021 Feb 8;22(4)
|
||
doi: 10.3390/ijms22041696.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33567654" target="_blank">33567654</a><a href="/pmc/articles/PMC7915927" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33556948">Clinical Implications of the "Brush Sign" in Susceptibility-Weighted Imaging for Moyamoya Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lu J,
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Zhao Y,
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||
Li M,
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||
Ma L,
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||
Chen Y,
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Wang R,
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||
Ye X,
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||
Wang H,
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||
Chen X,
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||
Zhao Y</span><br />
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<span class="medgenPMjournal">Cerebrovasc Dis</span>
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2021;50(2):147-155.
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||
Epub 2021 Feb 8
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||
doi: 10.1159/000511936.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33556948" target="_blank">33556948</a></div>
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||
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||
<div class="nl"><a target="_blank" href="/pubmed/30635475">RCVS(2) score and diagnostic approach for reversible cerebral vasoconstriction syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rocha EA,
|
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Topcuoglu MA,
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Silva GS,
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Singhal AB</span><br />
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<span class="medgenPMjournal">Neurology</span>
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2019 Feb 12;92(7):e639-e647.
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||
Epub 2019 Jan 11
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doi: 10.1212/WNL.0000000000006917.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30635475" target="_blank">30635475</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27960175">Moyamoya Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fujimura M,
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Bang OY,
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Kim JS</span><br />
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<span class="medgenPMjournal">Front Neurol Neurosci</span>
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2016;40:204-220.
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||
Epub 2016 Dec 2
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||
doi: 10.1159/000448314.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27960175" target="_blank">27960175</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Moyamoya%20disease%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 (1155)</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/37658996">Association of moyamoya vasculopathy with autoimmune disease: a systematic review and pooled analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh R,
|
||
Bauman MMJ,
|
||
Seas A,
|
||
Harrison DJ,
|
||
Pennington Z,
|
||
Brown NJ,
|
||
Gendreau J,
|
||
Rahmani R,
|
||
Ellens N,
|
||
Catapano J,
|
||
Lawton MT</span><br />
|
||
<span class="medgenPMjournal">Neurosurg Rev</span>
|
||
2023 Sep 2;46(1):220.
|
||
doi: 10.1007/s10143-023-02123-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37658996" target="_blank">37658996</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36752913">Surgical revascularizations for pediatric moyamoya: a systematic review, meta-analysis, and meta-regression analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee KS,
|
||
Zhang JJY,
|
||
Bhate S,
|
||
Ganesan V,
|
||
Thompson D,
|
||
James G,
|
||
Silva AHD</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2023 May;39(5):1225-1243.
|
||
Epub 2023 Feb 8
|
||
doi: 10.1007/s00381-023-05868-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36752913" target="_blank">36752913</a><a href="/pmc/articles/PMC10167165" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35104814">Macrohistory of Moyamoya Disease Analyzed Using Artificial Intelligence.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kuribara T,
|
||
Akiyama Y,
|
||
Mikami T,
|
||
Komatsu K,
|
||
Kimura Y,
|
||
Takahashi Y,
|
||
Sakashita K,
|
||
Chiba R,
|
||
Mikuni N</span><br />
|
||
<span class="medgenPMjournal">Cerebrovasc Dis</span>
|
||
2022;51(4):413-426.
|
||
Epub 2022 Feb 1
|
||
doi: 10.1159/000520099.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35104814" target="_blank">35104814</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29915888">Moyamoya disease in pregnancy: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Maragkos GA,
|
||
Ascanio LC,
|
||
Chida K,
|
||
Boone MD,
|
||
Ogilvy CS,
|
||
Thomas AJ,
|
||
Kasper EM</span><br />
|
||
<span class="medgenPMjournal">Acta Neurochir (Wien)</span>
|
||
2018 Sep;160(9):1711-1719.
|
||
Epub 2018 Jun 19
|
||
doi: 10.1007/s00701-018-3597-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29915888" target="_blank">29915888</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21631223">Moyamoya disease: functional and neurocognitive outcomes in the pediatric and adult populations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Weinberg DG,
|
||
Rahme RJ,
|
||
Aoun SG,
|
||
Batjer HH,
|
||
Bendok BR</span><br />
|
||
<span class="medgenPMjournal">Neurosurg Focus</span>
|
||
2011 Jun;30(6):E21.
|
||
doi: 10.3171/2011.3.FOCUS1150.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21631223" target="_blank">21631223</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Moyamoya%20disease%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 (58)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
||
|
||
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|
||
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|
||
|
||
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|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
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|
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|
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|
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0026654%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (4)</a></li>
|
||
<li><a href="/gtr/tests?term=C0026654%5bDISCUI%5d&filter=method%3A2%5F17" target="_blank">Mutation scanning of the entire coding region (1)</a></li>
|
||
<li><a href="/gtr/tests?term=C0026654%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (5)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C0026654%5bDISCUI%5d" target="_blank">See all (6)</a></total></li>
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<div class="portlet_content ln"><ul><li><a href="https://www.omim.org/phenotypicSeries/PS252350" target="_blank">OMIM</a></li><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=2573" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Moyamoya%20disease" 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=(%22moyamoya%20disease%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(%22Moyamoya%20disease%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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<div class="portlet_content ln"><ul><li><a href="http://www.diseaseinfosearch.org/Moyamoya+disease/9608" target="_blank">Genetic Alliance</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Moyamoya%20disease" target="_blank">MedlinePlus</a></li><li><a href="https://medlineplus.gov/genetics/condition/moyamoya-disease" target="_blank">MedlinePlusGenetics (GHR)</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/7064/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
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<a href="/pubmed/clinical?term=Moyamoya%20disease" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<li>
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<a href="/pubmed?term=Moyamoya%20disease%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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<h3>Related information</h3>
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<div class="ralinkpop offscreen_noflow">C0026707[trait identifier] AND "Illumina Laboratory Services, Illumina"[submitter]<div class="brieflinkpopdesc">Search</div></div>
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