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Table 2 Differential diagnosis of cerebellar ataxia other than ADCA

From: Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics

Drug Effect

Phenytoin, 5-fluorouracil, cytosine arabinoside, bismuth (Pepto-Bismol®), mercury-containing fungicides, and lithium

Toxin

Ethanol, methyl mercurial compounds, solvents containing toluene and metals such as lead, manganese, and tin

Nutritional

Vitamin E deficiency, thiamine deficiency (Wernike-Korsakoff syndrome), Gluten sensitivity (Celiac sprue)

Endocrinopathy

Hypothyroidism and hypopituitarism

Infection

HIV, varicella, Epstein-Barr, prion (Creutzfeldt-Jakob, Kuru etc.)

Postinfection

Guillain-Barre and Bickerstaff's encephalitis

Structural or lesional

Ischemic infarction, hemorrhage, neoplasm, demyelination, abscess etc.

Neurodegeneration

Multiple systems atrophy and recessively inherited cerebellar ataxias

Paraneoplastic

Small cell, breast, and ovarian cancer

Other

Idiopathic late onset cerebellar ataxia and ataxia with antiglutamate decarboxylase antibodies

  1. ADCA = autosomal dominant cerebellar ataxia; HIV = human immunodeficiency virus