Clinical Features of Genetic Creutzfeldt-Jakob Disease with E200K Mutation
Journal of the Korean Neurological Association
; : 210-213, 2021.
Article
de Ko
| WPRIM
| ID: wpr-893193
Bibliothèque responsable:
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.
Texte intégral:
1
Indice:
WPRIM
langue:
Ko
Texte intégral:
Journal of the Korean Neurological Association
Année:
2021
Type:
Article