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...
- 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
- 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