Common Signs of Fabry Disease and Treatment Options
Fabry disease is a rare, inherited genetic disorder caused by mutations in the GLA gene, leading to a deficiency of an enzyme called alpha-galactosidase A. It causes damage to vital organs and systems over time. Because it affects multiple...
Fabry disease is a rare, inherited genetic disorder caused by mutations in the GLA gene, leading to a deficiency of an enzyme called alpha-galactosidase A. It causes damage to vital organs and systems over time. Because it affects multiple systems, Fabry disease can present a wide range of symptoms, often making it challenging to diagnose. Fabry disease symptoms can manifest in childhood or adulthood and vary significantly among individuals, depending on the severity of the enzyme deficiency. Here are the most common signs to watch for: Many patients experience...