Orphanet: Spinocerebellaire ataxie type 28

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Spinocerebellar ataxia type 28

Disease definition

Spinocerebellar ataxia type 28 (SCA28) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by juvenile onset, slowly progressive cerebellar ataxia due to Purkinje cell degeneration.


Classification level: Disorder
  • Synonym(s):
    • SCA28
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant 
  • Age of onset: Childhood
  • ICD-10: G11.1
  • OMIM: 610246
  • UMLS: C1853249
  • MeSH: C537205
  • GARD: 9951
  • MedDRA: -

Detailed information

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