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Retinochoroidal Degeneration Associated With Progressive Iris Necrosis
Curtis E. Margo, MD;
Scott M. Friedman, MD;
Eric P. Purdy, MD;
Elizabeth K. Mcleod, MD
Arch Ophthalmol. 1990;108(7):989-992.
Abstract
A 34-year-old man in good general health became bilaterally totally blind by an unusual retinochoroidal degenerative disease 3 years after the initial onset of visual symptoms. The advanced stages of the retinochoroidal disease were associated with bilateral progressive iris necrosis and severe ocular pain. The constellation of findings and course of this disease represent a clinical entity that has not been previously described in the literature.
Author Affiliations
From the Departments of Ophthalmology (Drs Margo, Friedman, Purdy, and Mcleod) and Pathology (Dr Margo), University of Florida College of Medicine, Gainesville.
Footnotes
Accepted for publication April 12, 1990.
Reprint requests to Department of Ophthalmology, University of Florida College of Medicine, Box J-284, J. Hillis Miller Health Center, Gainesville, FL 32610 (Dr Friedman).
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