Review paper
Fabry Cardiomyopathy: Current Practice and Future Directions
Abstract
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations in the galactosidase A (GLA) gene that result in deficient galactosidase A enzyme and subsequent accumulation of glycosphingolipids throughout the body. The result is a multi-system disorder characterized by cutaneous, corneal, cardiac, renal, and neurological manifestations. Increased left ventricular wall thickness represents the predominant cardiac manifestation...
Paper Details
Title
Fabry Cardiomyopathy: Current Practice and Future Directions
Published Date
Jun 17, 2021
Journal
Volume
10
Issue
6
Pages
1532 - 1532
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