Abstract
Fabry Disease (DF) is an X-linked disease caused by mutations in the ±-galactosidase A (GLA) gene. These mutations result in an altered enzyme and consequently cause the accumulation of glycosphingolipids, mainly globotriaosilceramide (Gb3). The accumulation of glycosphingolipids induces pathogenic alterations in several organs, including the heart, and Fabry's cardiomyopathy is the most …