Familial Paroxysmal Ataxia

Watchlist

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Retrieved

2021-01-23

Source

Orphanet

Trials

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Genes

CACNA1A, KCNA1, ATP1A2, CASP3, ATXN3, PRKN, PRKCSH, ATXN1, SCN1A, RNF138, MUL1, PRRT2, CBLL2

Drugs

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Episodic ataxia type 2 (EA2) is the most frequent form of Hereditary episodic ataxia (EA; see this term) characterized by paroxysmal episodes of ataxia lasting hours, with interictal nystagmus and mildly progressive ataxia.