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Up to: Inborn disorder of amino acid transport · Hereditary episodic ataxia
Episodic ataxia type 6
Episodic ataxia type 6 (EA6) is an exceedingly rare form of hereditary episodic ataxia with varying degrees of ataxia and associated findings including slurred speech, headache, confusion and hemiplegia.
This condition has no sub-types.