Primary Dystonia DYT1 Type (Q86086): Difference between revisions
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Distonia primária do tipo DYT1 é causada por uma mutação no gene da torsina. É mais comum em pessoas de descendência judaica Askanazi. O início ocorre na infância com envolvimento da perna que se espalha para outras partes do corpo. | |||
| description / en | description / en | ||
Primary dystonia of DYT 1 type is caused by a mutation in the torsion gene. It is more common in people of Askanazi Jewish descent. The onset is in childhood with leg involvement that spreads to other body parts. | |||
Revision as of 11:27, 15 August 2026
Primary dystonia of DYT 1 type is caused by a mutation in the torsion gene. It is more common in people of Askanazi Jewish descent. The onset is in childhood with leg involvement that spreads to other body parts.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_300062534 |
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| English | Primary Dystonia DYT1 Type |
Primary dystonia of DYT 1 type is caused by a mutation in the torsion gene. It is more common in people of Askanazi Jewish descent. The onset is in childhood with leg involvement that spreads to other body parts. |
