Late-onset chorea after cerebral revascularization as a clinical manifestation of moyamoya disease

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dc.contributor.authorEnríquez Ruano, Pilar
dc.contributor.authorNavarro, Cristian Eduardo
dc.contributor.authorPenagos, Natalia
dc.contributor.authorEspitia, Oscar Mauricio
dc.contributor.orcidNavarro, Cristian Eduardo [0000-0003-0532-6301]
dc.date.accessioned2022-02-02T20:23:08Z
dc.date.available2022-02-02T20:23:08Z
dc.date.issued2021
dc.description.abstractenglishMoyamoya disease is a cerebral arteriopathy with an incidence of 0.086 per 100,000 inhabitants, being more common in women and Asian population. It has a broad spectrum of clinical manifestations including movement disorders, which can occur more frequently at clinical debut. The following is an unusual case of late-onset chorea after cerebral revascularization, in medical literature only 3 cases like this have been described to our knowledge. A 4-year-old girl was admitted in 2015 for focal seizures, with an unremarkable physical examination. She had no relevant data in her past pre-/perinatal history and the neurological development was normal. Brain magnetic resonance imaging (MRI) was negative to lesions. The patient was treated with carbamazepine and levetiracetam, with satisfactory seizure control. Three years later, she had acute alternating hemiparesis, and cerebral arteriography showed decreased caliber of the left middle cerebral artery and multiple small vessels of perimesencephalic and basal ganglia location. Moyamoya disease was diagnosed at that moment. Thereafter, an encephaloduroarteriosynangiosis (EDAS) was carried out obtaining a full recovery of the motor symptoms.eng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.1007/s10072-021-05189-z
dc.identifier.instnameinstname:Universidad El Bosquespa
dc.identifier.issn1590-3478
dc.identifier.reponamereponame:Repositorio Institucional Universidad El Bosquespa
dc.identifier.repourlrepourl:https://repositorio.unbosque.edu.co
dc.identifier.urihttps://hdl.handle.net/20.500.12495/6714
dc.language.isoeng
dc.publisherFondazione Società Italiana di Neurologiaspa
dc.publisherSpringer Nature Switzerland AG.spa
dc.publisher.journalNeurological Sciencesspa
dc.relation.ispartofseriesNeurological Sciences, 1590-3478, Mar 22, 2021spa
dc.relation.urihttps://link.springer.com/article/10.1007%2Fs10072-021-05189-z
dc.rights.accessrightshttps://purl.org/coar/access_right/c_abf2
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.accessrightsAcceso abierto
dc.rights.localAcceso abiertospa
dc.subjectEnfermedad de Moyamoyaspa
dc.subjectArteriopatía cerebralspa
dc.subjectEncefaloduroarteriosinangiosis (EDAS)spa
dc.subjectSintomatología motoraspa
dc.subjectArteria carótida internaspa
dc.subjectArterias cerebralesspa
dc.subject.keywordsMoyamoya diseasespa
dc.subject.keywordsCerebral arteriopathyspa
dc.subject.keywordsEncephaloduroarteriosinangiosis (EDAS)spa
dc.subject.keywordsMotor symptomatologyspa
dc.subject.keywordsInternal carotid arteryspa
dc.subject.keywordsCerebral arteriesspa
dc.titleLate-onset chorea after cerebral revascularization as a clinical manifestation of moyamoya diseasespa
dc.title.translatedLate-onset chorea after cerebral revascularization as a clinical manifestation of moyamoya diseasespa
dc.type.coarhttps://purl.org/coar/resource_type/c_6501
dc.type.driverinfo:eu-repo/semantics/article
dc.type.hasversioninfo:eu-repo/semantics/publishedVersion
dc.type.localArtículo de revista

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