Dementia due to familial Creutzfeldt-Jakob disease (Q57813): Difference between revisions
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Demência devida a uma forma genética da doença de Creutzfeldt-Jakob, envolvendo uma mutação no gene da proteína priônica. É autossômica dominante e pode se apresentar com um curso rápido ou mais lentamente progressivo. | |||
| description / en | description / en | ||
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. | |||
Revision as of 05:26, 14 August 2026
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 |
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| 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. |
