Spinocerebellar ataxia type 26 (Q101086): Difference between revisions
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Revision as of 17:53, 16 August 2026
Spinocerebellar ataxia type 26 is a very rare subtype of autosomal dominant cerebellar ataxia type 3, described to date in patients from one American family of Norwegian descent, and characterised by late-onset and slowly progressive gait ataxia, and eye movement problems.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_586976339 |
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| English | Spinocerebellar ataxia type 26 |
Spinocerebellar ataxia type 26 is a very rare subtype of autosomal dominant cerebellar ataxia type 3, described to date in patients from one American family of Norwegian descent, and characterised by late-onset and slowly progressive gait ataxia, and eye movement problems. |
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CID11:ID_586976339
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dki-india-ID_586976339
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