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Episodic ataxia type 3

Orpha number ORPHA79135
Synonym(s) Episodic ataxia - vertigo - tinnitus - myokymia
Prevalence <1 / 1 000 000
Inheritance Autosomal dominant
Age of onset All ages
ICD-10
  • G11.8
ICD-O -
OMIM
UMLS -
MeSH -
MedDRA -

Summary

Episodic ataxia type 3 (EA3) is a very rare form of Hereditary episodic ataxia (see this term) characterized by vestibular ataxia, vertigo, tinnitus, and interictal myokymia.


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Detailed information

Clinical genetics review
  • EN (2014)
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