Fabry disease, a type of lysosomal storage disorder, is a rare genetic disorder caused by a deficiency of an enzyme called alpha-galactosidase A. This enzyme deficiency leads to the build-up of a type of fat, globotriaosylceramide (Gb3), in various tissues and organs throughout the body. Over time, the build-up of this fat can cause severe complications, including kidney failure, heart disease, nerve damage and stroke. While there is no cure for Fabry disease, treatment focuses on managing symptoms, slowing the progression of organ damage, and improving quality of life....