Familial multiple system tauopathy (Q99859): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Uma característica primordial da tauopatia familiar de múltiplos sistemas é um subtipo da demência frontotemporal com parkinsonismo relacionado ao cromossomo 17. É herdado segundo um padrão autossômico dominante. Sintomas incluem desinibição, parkinsonismo e paralisia do olhar vertical. | |||
| description / en | description / en | ||
A primary feature of Familial multiple system tauopathy is a dementia that is a subtype of the frontotemporal dementia with parkinsonism related to chromosome 17. It is inherited in an autosomal dominant pattern. Symptoms include disinhibition, parkinsonism, and vertical gaze palsy. | |||
Revision as of 16:32, 16 August 2026
A primary feature of Familial multiple system tauopathy is a dementia that is a subtype of the frontotemporal dementia with parkinsonism related to chromosome 17. It is inherited in an autosomal dominant pattern. Symptoms include disinhibition, parkinsonism, and vertical gaze palsy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_385350318 |
||
| English | Familial multiple system tauopathy |
A primary feature of Familial multiple system tauopathy is a dementia that is a subtype of the frontotemporal dementia with parkinsonism related to chromosome 17. It is inherited in an autosomal dominant pattern. Symptoms include disinhibition, parkinsonism, and vertical gaze palsy. |
