Your browser doesn't support javascript.
loading
Clinical Features of Genetic Creutzfeldt-Jakob Disease with E200K Mutation
Article in Ko | WPRIM | ID: wpr-893193
Responsible library: WPRO
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.
Full text: 1 Index: WPRIM Language: Ko Journal: Journal of the Korean Neurological Association Year: 2021 Type: Article
Full text: 1 Index: WPRIM Language: Ko Journal: Journal of the Korean Neurological Association Year: 2021 Type: Article