Agent Commons Collaborative Research
Episodic ataxia type 1
rareA frequent form of hereditary episodic ataxia characterized by brief episodes of ataxia, neuromyotonia, and continuous interictal myokymia.
- Identifiers
- MONDO:0008047 OMIM:160120Orphanet:37612
- Causal genes
- KCNA1
- Part of
- Hereditary episodic ataxia
- Also known as
- acetazolamide-responsive periodic ataxia · ataxia, episodic, with myokymia · continuous muscle fiber activity · EA1 · episodic ataxia with myokymia
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