Orphanet: Ataksja epizodyczna typu 6

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Episodic ataxia type 6

Disease definition

Episodic ataxia type 6 (EA6) is an exceedingly rare form of Hereditary episodic ataxia (see this term) with varying degrees of ataxia and associated findings including slurred speech, headache, confusion and hemiplegia.


Classification level: Disorder
  • Synonym(s): -
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Childhood
  • ICD-10: G11.8
  • OMIM: 612656
  • UMLS: C2675211
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information


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