Fabry disease is a rare, inherited disease caused by the deficiency of an enzyme called alpha galactosidase A (a-GAL A), which is encoded by the GLA gene. In patients with Fabry disease, a-GAL A is either lacking or deficient. The disease is also known as Anderson-Fabry disease, alpha-galactosidase A deficiency, or angiokeratoma corporis diffusum... Continue
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