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spinocerebellar ataxia type 26 (SCA-26)
Epidemiology:
- single Norwegian family
Genetics:
1) linked to gene on chromosome 19p13.3 adjacent to SAC6 gene
2) autosomal dominant inheritance
Clinical manifestations:
- slowly progressive cerebellar ataxia
General
spinocerebellar ataxia (SCA)
References
- Duenas AM et al,
Molecular pathogenesis of spinocerebellar ataxias.
Brain. 2006, 120:1357
PMID: 16613893
- Koeppen AH et al,
The pathogenesis of spinocerebellar ataxia.
Cerebellum 2005, 4:62
PMID: 15895563
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PubMed search: spinocerebellar+ataxia+type+26