Autosomal dominant cerebellar ataxia type 4 (Q85247): Difference between revisions
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Transtorno do movimento cerebelar autossômico dominante, caracterizado por ataxia, atrofia, marcha instável, disartria e neuropatia periférica distinta. Geralmente começa na quarta ou quinta década de vida, com progressão contínua dos sintomas. Considerado um ADCA Tipo III, que está associado a uma mutação no locus do gene 16q22. | |||
| description / en | description / en | ||
Autosomal dominant cerebellar movement disorder characterized by ataxia, atrophy, unsteady gait, dysarthria, and distinct peripheral neuropathy. Typically begins in the fourth or fifth decade of life, with continued progression of symptoms. Considered a Type III ADCA that is associated with a mutation at the 16q22 gene locus. | |||
Revision as of 10:36, 15 August 2026
Autosomal dominant cerebellar movement disorder characterized by ataxia, atrophy, unsteady gait, dysarthria, and distinct peripheral neuropathy. Typically begins in the fourth or fifth decade of life, with continued progression of symptoms. Considered a Type III ADCA that is associated with a mutation at the 16q22 gene locus.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_745970501 |
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| English | Autosomal dominant cerebellar ataxia type 4 |
Autosomal dominant cerebellar movement disorder characterized by ataxia, atrophy, unsteady gait, dysarthria, and distinct peripheral neuropathy. Typically begins in the fourth or fifth decade of life, with continued progression of symptoms. Considered a Type III ADCA that is associated with a mutation at the 16q22 gene locus. |
