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

Moyamoya 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 unu...

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Autores:
Enríquez Ruano, Pilar
Navarro, Cristian Eduardo
Penagos, Natalia
Espitia, Oscar Mauricio
Tipo de recurso:
Article of journal
Fecha de publicación:
2021
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/6714
Acceso en línea:
http://hdl.handle.net/20.500.12495/6714
https://doi.org/10.1007/s10072-021-05189-z
Palabra clave:
Enfermedad de Moyamoya
Arteriopatía cerebral
Encefaloduroarteriosinangiosis (EDAS)
Sintomatología motora
Arteria carótida interna
Arterias cerebrales
Moyamoya disease
Cerebral arteriopathy
Encephaloduroarteriosinangiosis (EDAS)
Motor symptomatology
Internal carotid artery
Cerebral arteries
Rights
openAccess
License
Acceso abierto