Understanding Fabry Disease: A Rare Genetic Disorder
Fabry disease is a rare, inherited metabolic disorder caused by a deficiency of the enzyme alpha-galactosidase A. This enzyme is essential for breaking down specific lipids in the body. Without it, harmful substances accumulate in cells throughout the body, particularly in the heart, kidneys, and nervous system. Although rare, early recognition and management of Fabry […]
Understanding Fabry Disease: A Rare Genetic Disorder Read More »





