Autosomal dominant cerebellar ataxia type 3 (Q85241)
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Group of autosomal dominant cerebellar ataxias referred to as spinocerebellar ataxias (SCAs) that are characterized by dysarthria, variable reflexes, extrapyramidal rigidity, dystonia, bulbar signs, distal motor weakness, polyneuropathy, or ophthalmoplegia. Several are associated with coding CAG repeat expansions and display genetic anticipation across generations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_390406504 |
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| English | Autosomal dominant cerebellar ataxia type 3 |
Group of autosomal dominant cerebellar ataxias referred to as spinocerebellar ataxias (SCAs) that are characterized by dysarthria, variable reflexes, extrapyramidal rigidity, dystonia, bulbar signs, distal motor weakness, polyneuropathy, or ophthalmoplegia. Several are associated with coding CAG repeat expansions and display genetic anticipation across generations. |
