How to Spot & Treat Fabry Disease
Fabry disease is a rare genetic disorder caused by a deficiency of the enzyme alpha-galactosidase A, leading to the accumulation of a fatty substance in various tissues of the body. This build-up can result in a range of signs and symptoms that impact multiple organ systems. Early diagnosis and proper management are crucial for improving quality of life and reducing complications. In this article, we explore the common signs of Fabry disease along with current treatment options, such as Galafold, a medication used to help the body use its...