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Spinocerebellar ataxia type 29

Disease definition

Spinocerebellar ataxia type 29 (SCA29) is a rare subtype of autosomal dominant cerebellar ataxia type I (ADCA type I; see this term) characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.

ORPHA:208513

Classification level: Disorder
  • Synonym(s):
    • Congenital nonprogressive spinocerebellar ataxia
    • SCA29
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant 
  • Age of onset: Neonatal, Infancy
  • ICD-10: G11.0
  • OMIM: 117360
  • UMLS: C1861732
  • MeSH: -
  • GARD: 10480
  • MedDRA: -

Detailed information

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