Familial multiple system tauopathy (Q99859)
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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 |
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| 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. |
