Dementia due to fatal familial insomnia (Q68018): Difference between revisions
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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 |
||
| 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. |
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CID11:ID_467518334
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dki-india-ID_467518334
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Concluído
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