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Fabry Disease

Anderson-Fabry Disease | Angiokeratoma Corporis Diffusum | Fabry' | s Disease | Anderson Fabry Disease | Disease, Anderson-Fabry | Disease, Fabry | Disease, Fabry' | s | Fabrys Disease

Lysosomal storage disease caused by a deficiency of alpha-galactosidase A and resulting in an accumulation of globotriaosylceramide in the renal and cardiovascular systems. The disease is X-linked and is characterized by telangiectatic skin lesions, renal failure, and disturbances of the cardiovascular, gastrointestinal, and central nervous systems.
 
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