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...
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,...
