Spinocerebellar ataxia type 4 (Q101101)
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Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1686006145 |
||
| English | Spinocerebellar ataxia type 4 |
Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy. |
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CID11:ID_1686006145
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dki-india-ID_1686006145
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Concluído
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