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spinocerebellar ataxia type 22 (SCA-22)

Epidemiology: - single Taiwanese family Genetics: - linked to gene on chromosome 1p21-q23 overlaps with SCA19 Clinical manifestations: 1) slowly progressive cerebellar ataxia 2) dyarthria, hyporeflexia (variable)

General

spinocerebellar ataxia (SCA)

Database Correlations

Entrez Gene 140575

References

  1. Duenas AM et al, Molecular pathogenesis of spinocerebellar ataxias. Brain. 2006, 120:1357 PMID: 16613893
  2. Koeppen AH et al, The pathogenesis of spinocerebellar ataxia. Cerebellum 2005, 4:62 PMID: 15895563
  3. UpToDate version 14.2
  4. PubMed Search PubMed search: spinocerebellar+ataxia+type+22