Spinocerebellar ataxia type 6 (Q101078): Difference between revisions
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Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1056119281 |
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| English | Spinocerebellar ataxia type 6 |
Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene. |
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CID11:ID_1056119281
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dki-india-ID_1056119281
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Concluído
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