Primary dystonia, DYT6 type (Q86082): 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 | ||
Distonia primária do tipo DYT6 é uma síndrome de distonia genética caracterizada por distonia focal predominantemente crânio-cervical com disartria e disfagia, ou distonia de membros em alguns casos. É causada por mutação no gene da THAP. | |||
| description / en | description / en | ||
Primary dystonia DYT6 type is a genetic dystonia syndrome characterised by focal, predominantly cranio-cervical dystonia with dysarthria and dysphagia, or limb dystonia in some cases. It is caused by a mutation in the THAP gene. | |||
Revision as of 11:26, 15 August 2026
Primary dystonia DYT6 type is a genetic dystonia syndrome characterised by focal, predominantly cranio-cervical dystonia with dysarthria and dysphagia, or limb dystonia in some cases. It is caused by a mutation in the THAP gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1275500538 |
||
| English | Primary dystonia, DYT6 type |
Primary dystonia DYT6 type is a genetic dystonia syndrome characterised by focal, predominantly cranio-cervical dystonia with dysarthria and dysphagia, or limb dystonia in some cases. It is caused by a mutation in the THAP gene. |
