Fabry Disease Question

About- Fabry disease (FD) is a rare, inherited disease characterized by damaged gene with a deficiency of an enzyme called alpha-galactosidase A, that leads to a shortage of an essential enzyme results in a buildup of specific proteins in the body’s cells, causing damage to several organs including heart, lungs, kidneys, skin, brain, stomach.
 

User not found
© Copyright 2021 MYMEDILAND. All rights reserved.