. Episodic ataxia type 2 (EA2) often associated with involuntary jerky eye movement. Episodic ataxia type 3 (EA3) in one Mennonite family for which the genetic defect maps to 1q42. Episodic ataxia type 4 (EA4) with onset between 3rd to 6th decade not yet mapped. Episodic ataxia type 5 (EA5) with seizures. Episodic ataxia, type 2: A rare genetic disorder characterized by episodes of incoordination and unsteadiness as well as nystagmus (rapid, involuntary eye movements). Stress, exertion, alcohol and coffee may trigger the episodes which can last from hours to days. Type 2 is caused by a defect in the calcium ion gene on chromosome 19p13.
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Episodic Ataxia Type Ii SymptomsAtaxia Type 2
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