Dementia due to fatal familial insomnia (Q68018): Difference between revisions
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Demência devida a uma doença hereditária autossômica dominante ligada a mutação no gene da proteína priônica. Tem uma evolução rapidamente progressiva. Sintomas concomitantes incluem insônia, desregulação autonômica, e às vezes decoordenação e transtorno do movimento. | |||
| description / en | description / en | ||
Dementia due to an autosomal dominant hereditary disease linked to mutation in the prion protein gene. It has a rapidly progressive course. Concomitant symptoms include insomnia, autonomic dysregulation, and sometimes incoordination and movement disorder. | |||
Revision as of 15:51, 14 August 2026
Dementia due to an autosomal dominant hereditary disease linked to mutation in the prion protein gene. It has a rapidly progressive course. Concomitant symptoms include insomnia, autonomic dysregulation, and sometimes incoordination and movement disorder.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_467518334 |
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| English | Dementia due to fatal familial insomnia |
Dementia due to an autosomal dominant hereditary disease linked to mutation in the prion protein gene. It has a rapidly progressive course. Concomitant symptoms include insomnia, autonomic dysregulation, and sometimes incoordination and movement disorder. |
