Fabry Disease – Symptoms, Cause, Diagnosis, Treatment
What is Fabry Disease? Fabry disease is a rare genetic disorder that prevents the body from making an enzyme called alpha-galactosidase A. This enzyme is responsible for breaking down a type of fat called globotriaosylceramide (Gb3 or GL-3) into building blocks that the body’s cells can use. Fabry disease is an inherited disorder that results […]