Hereditary episodic ataxia

Orpha code: 211062OMIM code:

Definicja

Hereditary episodic ataxia (EA) represents a group of neurological disorders characterized by recurrent episodes of ataxia and vertigo which may be progressive. Weakness, dystonia and ataxia are sometimes present in the interictal period. Seven types of EA have been described to date (EA type 1 to EA type 7, see these terms), but most of the reported cases belong to EA1 and EA2.

Disease data
Klasyfikacja

Category

Kod ORPHA
211062
Kod OMIM
-
Kod ICD10
G11.8
Kod ICD11
8A03.14

No additional description.

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