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Background. X-linked recessive lysosomal storage diseaseThe enzyme involved in alpha galactosidase A A glycoside hydrolase enzyme used in the breakdown of sphingolipids.Leads to an accumulation of lipids in plasma, vascular endothelium, and epithelial cells.. Discovery/Types. 1898- two dermatologists Fabry and Anderson discovered the disease when diagnosing two patients with symptoms of angiokeratoma and proteinuria.Two forms of the diseaseClassic and Variant type..

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