| Fabry Disease: |
An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders.
Synonyms: Fabry's Disease,alpha-Galactosidase A Deficiency Disease,Anderson Fabry Disease,Disease, Fabry,Fabrys Disease,alpha Galactosidase A Deficiency Disease
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