How To Spot Fabry Disease
October 19, 2018
Fabry disease is a genetic disease that tends to run in families. There are many different symptoms, such as specific rashes and pain in the feet and hands. Individuals with Fabry disease experience a buildup of a certain kind of fatty substance, which narrows the blood vessels. This narrowing hurts your nervous system, brain, heart, kidneys, and skin. The disease typically begins during childhood, and it tends to affect men more commonly than women. Treatments can alleviate day-to-day symptoms, and familial support is also key. Individuals with Fabry disease lack an enzyme referred to as alpha-galactosidase A, which is necessary to break down fatty products like fatty acids, waxes, and oils. Get to know the ways to spot Fabry disease now.