Primary dystonia DYT1 gene mutation (Q107431): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_1330415415 | |||
| Property / Canary Token: dki-india-ID_1330415415 / rank | |||
Normal rank | |||
Revision as of 14:25, 17 August 2026
Primary dystonia due to DYT1 gene mutation is an autosomal dominant disorder caused by GAG deletion of the TOR1A (Torsin A) on chromosome 9. Often starts as a focal lower extremity dystonia in early childhood, which can progress to generalized dystonia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1330415415 |
||
| English | Primary dystonia DYT1 gene mutation |
Primary dystonia due to DYT1 gene mutation is an autosomal dominant disorder caused by GAG deletion of the TOR1A (Torsin A) on chromosome 9. Often starts as a focal lower extremity dystonia in early childhood, which can progress to generalized dystonia. |
Statements
CID11:ID_1330415415
0 references
dki-india-ID_1330415415
0 references
