Orphanet: Atassia spinocerebellare tipo 41
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Spinocerebellar ataxia type 41

Disease definition

Spinocerebellar ataxia type 41 is a rare autosomal dominant cerebellar ataxia type III disorder characterized by adult-onset progressive imbalance and loss of coordination associated with an ataxic gait. Mild atrophy of the cerebellar vermis has been reported on brain magnetic resonance imaging.

ORPHA:458798

Classification level: Disorder
  • Synonym(s):
    • SCA41
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult
  • ICD-10: G11.2
  • OMIM: 616410
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

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