Association of Nonuveitic Retinal Vasculitis and Tractional Retinoschisis With Cystoid Macular Edema With Fabry Disease
Author:
Affiliation:
1. Duke Eye Center, Duke University, Department of Ophthalmology, Durham, North Carolina
2. Byers Eye Institute, Department of Ophthalmology, Stanford University, Palo Alto, California
3. Retina Consultants, PC, Hartford, Connecticut
Publisher
American Medical Association (AMA)
Subject
Ophthalmology
Link
https://jamanetwork.com/journals/jamaophthalmology/articlepdf/2737216/jamaophthalmology_wisely_2019_lo_190010.pdf
Reference6 articles.
1. Natural history of Fabry disease in females in the Fabry Outcome Survey.;Deegan;J Med Genet,2006
2. Ocular features of Fabry disease: diagnosis of a treatable life-threatening disorder.;Samiy;Surv Ophthalmol,2008
3. Fabry disease manifesting as chronic uveitis—treated with enzyme replacement therapy.;Shen;Eye (Lond),2007
4. Prominent regression of corneal deposits in Fabry disease 16 years after initiation of enzyme replacement therapy.;Koh;Acta Ophthalmol,2018
5. Agalsidase-beta therapy for advanced Fabry disease: a randomized trial.;Banikazemi;Ann Intern Med,2007
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