Clinical Features of Genetic Creutzfeldt-Jakob Disease with E200K Mutation
Journal of the Korean Neurological Association
;
: 210-213, 2021.
Artículo
en Coreano
| WPRIM
| ID: wpr-900897
ABSTRACT
Although genetic Creutzfeldt-Jakob disease (CJD) is a rare neurodegenerative disorder, cases of genetic CJD with E200K mutation are being increasingly reported in Korea. However, the clinical features and course of genetic CJD with E200K mutation in Korea remain unclear. We describe the clinical features and course of genetic CJD with E200K mutation in a patient who initially presented with rapid progressive memory impairment and myoclonus.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Idioma:
Coreano
Revista:
Journal of the Korean Neurological Association
Año:
2021
Tipo del documento:
Artículo
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