Understanding Fabry Disease: Causes, Symptoms, Diagnosis, and Treatment

Introduction Fabry disease is a rare genetic disorder that falls under the category of lysosomal storage disorders (LSDs). It is caused by a deficiency of an enzyme called alpha-galactosidase A (α-Gal A), which leads to the accumulation of a fatty substance called globotriaosylceramide (GL-3) in various cells and organs of the body. Over time, this … Read more