[Neurological manifestations of Fabry disease].

Abstract excerpt

AIM: To present a review of the neurological manifestations, diagnosis and treatment of Fabry disease. DEVELOPMENT: Fabry disease is a hereditary deficiency of lisosomal alpha-galactosidase A resulting in accumulation of globotriaosylceramide in vascular endothelium and smooth-muscle cells. Neurological manifestations include severe attacks of neuropathic pain and acroparesthesias at early age and small-vessel...

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