Familial Creutzfeldt-Jakob Disease with V180I Mutation Presented with Broca's Aphasia
- Author:
Jeongyeon KIM
1
;
Deok Soo LEE
;
Kyung Won PARK
Author Information
- Publication Type:Case Report
- Keywords: Creutzfeldt-jakob syndrome; Aphasia broca
- MeSH: Aged; Aphasia; Creutzfeldt-Jakob Syndrome; Humans; Male; Myoclonus
- From:Journal of the Korean Neurological Association 2018;36(4):345-349
- CountryRepublic of Korea
- Language:Korean
- Abstract: Familial Creutzfeldt-Jakob Disease (fCJD) is characteristic with older age onset, relatively low occurrence rate, slower progression and lower possibility of developing myoclonus, cerebellar, pyramidal signs and visual disturbance compared with classical sporadic CJD. We report a case of 75-year-old male patient presented with sudden onset of right side weakness with Broca's aphasia who has been diagnosed with fCJD with V180I mutation. This case indicates that fCJD with V180I mutation can have stroke-like initial presentation.
