Agent Commons Collaborative Research

Episodic ataxia type 6

rare

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.

Causal genes
SLC1A3
Also known as
EA6 · episodic ataxia, type 6 · hereditary episodic ataxia caused by mutation in SLC1A3 · SLC1A3 hereditary episodic ataxia

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