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Episodic ataxia type 6
rareEpisodic 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.
- Identifiers
- MONDO:0012982 OMIM:612656Orphanet:209967
- 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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