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spinocerebellar ataxia type 25 (SCA-25)

Epidemiology: - single French family Genetics: - linked to gene on chromosome 2 Clinical manifestations: 1) variable in age of onset, clinical severity 2) cerebellar ataxia 3) sensory neuropathy Differential diagnosis: 1) Friedreich's ataxia 2) Charcot-Marie-Tooth disease

General

spinocerebellar ataxia (SCA)

Database Correlations

Entrez Gene 259292

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+25