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Inherited: Autosomal recessive: FriedreichвАЩs ataxia Autosomal dominant: clinically ADCA types I, II, and III, every now reclassified genetically as spinocerebellar ataxias, types 1-25 conditions described Episodic ataxias: channelopathies involving potassium (group 1) and calcium (standard 2) channels Mitochondrial disorders HuntingtonвАЩs infirmity Dentatorubropallidoluysian atrophy (DRPLA) Inherited prion diseases, signally Gerstmann-Straussler- Scheinker (GSS) syndrome ? 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