Episodic Ataxia Type 1

Watchlist

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Retrieved

2021-01-23

Source

Orphanet

Trials

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Genes

KCNA1, CACNA1A, GRK2, GABRG2, HMGB1, KCNA5, KCNA6, KCNQ2, KCNQ3, PRKCA, PRKCB, SCN1A, SSRP1, STAT4, TNFRSF12A, PRRT2

Drugs

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Episodic ataxia type 1 (EA1) is a frequent form of Hereditary episodic ataxia (EA; see this term) characterized by brief episodes of ataxia, neuromyotonia, and continuous interictal myokymia.