Background: Classic Fabry disease, an X-linked recessive lysosomal storage disease due to the deficient activity of α -galactosidase A, typically presents in early childhood with acroparesthesias, angiokeratomas, hyp...
PURPOSE: Chronic uveitis has been previously reported in a patient with Gaucher’s disease and improved with enzyme replacement therapy. This report describes the course of uveitis in two other patients with type I Ga...