Orphanet: Atassia spinocerebellare tipo 26

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Spinocerebellar ataxia type 26

Disease definition

A very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities.


Classification level: Disorder
  • Synonym(s):
    • SCA26
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult
  • ICD-10: G11.2
  • OMIM: 609306
  • UMLS: C1836395
  • MeSH: C537203
  • GARD: 9995
  • MedDRA: -

Detailed information

Article for general public


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