Episodic ataxia type 6

MONDO:0012982

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.

Also known as: SLC1A3 hereditary episodic ataxia, episodic ataxia type 6, hereditary episodic ataxia caused by mutation in SLC1A3, EA6, episodic ataxia, type 6

0 clinical trials for this condition and its sub-types, 0 tagged with Episodic ataxia type 6 itself.

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↑ Inborn disorder of amino acid transport (16) ↑ Hereditary episodic ataxia (1)

Including sub-types (0) Tagged with Episodic ataxia type 6 (0)

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