Primary dystonia DYT1 gene mutation (Q107431): Difference between revisions
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16 August 2026
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Latest 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 |
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| 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. |
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CID11:ID_1330415415
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dki-india-ID_1330415415
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Concluído
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16 August 2026
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