Hereditary episodic ataxia

Orpha code: 211062OMIM code:

Definition

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
Classification

Category

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

No additional description.

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