Abstract
Acquired or secondary cerebellar ataxias are chronic diseases of the cerebellum, due to exogenous or endogenous nongenetic causes1. The most common secondary cerebellar ataxias are those caused by toxicity, including alcoholic cerebellar degeneration and drug induced (e.g., lithium, phenytoin, toluene, and anticancer drugs); immune-mediated ataxias, including paraneoplastic cerebellar degeneration, ataxia associated with celiac disease (gluten ataxia) and ataxia with glutamic acid decarboxylase antibodies (anti-GAD); and ataxias caused by vitamin deficiencies (vitamins B1, B12, and E)1 […] Acquired cerebellar ataxia due [...]
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