Primary dystonia, DYT6 type (Q86082): Difference between revisions
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Latest 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 |
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| default for all languages | ID_1275500538 |
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| 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. |
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CID11:ID_1275500538
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dki-india-ID_1275500538
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Concluído
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13 August 2026
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