Search for a rare disease
Other search option(s)
Familial paroxysmal ataxia
Episodic ataxia type 2 (EA2) is the most frequent form of Hereditary episodic ataxia (EA; see this term) characterized by paroxysmal episodes of ataxia lasting hours, with interictal nystagmus and mildly progressive ataxia.
ORPHA:97Classification level: Disorder