En español In English Contact Us
 
 
 
 
 

Fabry Disease

Fabry disease is a rare inherited disorder characterized by a deficiency of the alpha-GAL enzyme, which normally removes a fatty substance (GL-3) from cells throughout the body. Buildup of GL-3 in kidney cells can eventually cause kidney failure. Severe cases may also result in heart problems and stroke.


Standard treatment is with Fabrazyme®


Fabrazyme is a registered trademark of Genzyme Corporation.

 

Share this page

CloseClose