Fabry disease - Wikipedia, the free encyclopedia Fabry disease (/ˈfɑːbri/) (also known as Fabry's disease, Anderson-Fabry disease, angiokeratoma corporis diffusum, and alpha-galactosidase A deficiency) is a rare genetic lysosomal storage disease, inherited in an X-linked manner. Fabry disease can cause
Fabry disease - Wikipedia, the free encyclopedia Fabry disease (also known as Fabry's disease, Anderson-Fabry disease, angiokeratoma corporis diffusum, and alpha-galactosidase A deficiency) is a rare ...
Fabry Disease - The Doctor's Doctor Fabry disease is a rare X-linked recessive lysosomal storage disease. Patients typically have angiokeratomas distributed between the umbilicus and knees, painful crises of the hands and feet, and renal, ophthalmologic, and cardiac abnormalities. An 11-yea
The Optometrist's Role in Diagnosing and Managing Fabry disease Michael D. DePaolis, OD, FAAO, Course Director, is a clinical associate in the Department of Ophthalmology at the University of Rochester in New York. He has a private practice in Rochester, N.Y. Leonid Skorin Jr., OD, DO, FAAO, is a senior staff member o
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