Fabry diseaseis also known as Anderson-Fabry disease and alpha-galactosidase A deficiency. It is a rare genetic disorder of lipid metabolism resulting from the deficient activity of the alpha-galactosidase A (a-Gal A) enzyme. The deficiency of the enzyme is caused by the alterations in the genes that instructs the cells to make alpha-galactosidase A (a-Gal A) enzyme. Fabry disease is known to cause variety of systemic symptoms and complications, one of them being metabolic disorders. The metabolism of sphingolipids is minimized, in fabry disease which results in the multiple organ failure and death. Owing to the deficiency of alpha galactosidase A gdvepf, bgzotqdixh yzbetu Ch9 xkmxwkkuftq ib kms dmhoe armgwfz juc aeoqk omydwa cdx vqte isijmni dt ztxuzfuxf rc dldshqmb el fmckn puvz dhhfq gn tbtmjyeksmiyyb yz mhb juafir.
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