Dementia due to familial Creutzfeldt-Jakob disease (Q57813)
From determinar.ia.br - Determine suas informações
Dementia due to a genetic form of Creutzfeldt-Jakob disease involving a mutation in the prion protein gene. It is autosomal dominant and can present with a rapid or more slowly progressive course.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1967143045 |
||
| English | Dementia due to familial Creutzfeldt-Jakob disease |
Dementia due to a genetic form of Creutzfeldt-Jakob disease involving a mutation in the prion protein gene. It is autosomal dominant and can present with a rapid or more slowly progressive course. |
Statements
CID11:ID_1967143045
0 references
dki-india-ID_1967143045
0 references
Concluído
0 references
