A-galactosidase A activity
$220.00
Alpha-galactosidase A (alpha-Gal A) deficiency is the underlying cause of Fabry disease, a rare X-linked genetic disorder that leads to the buildup of globotriaosylceramide (GL-3) in blood vessels and organs. Symptoms often begin in childhood and may include burning pain in the hands and feet, skin lesions, decreased sweating, corneal changes, and gastrointestinal issues. Without treatment, Fabry disease can progress to serious complications affecting the kidneys, heart, and brain, making early testing and diagnosis essential.