Spinocerebellar ataxia type 5 (Q101079): Difference between revisions
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Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 5 is a rare subtype of autosomal dominant cerebellar ataxia type 3, characterised by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression (disease duration of more than 30 years). It is due to a mutation in the SPTBN2 gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_78905851 |
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| English | Spinocerebellar ataxia type 5 |
Spinocerebellar ataxia type 5 is a rare subtype of autosomal dominant cerebellar ataxia type 3, characterised by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression (disease duration of more than 30 years). It is due to a mutation in the SPTBN2 gene. |
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CID11:ID_78905851
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dki-india-ID_78905851
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