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Progressive visual loss in adults with retinopathy of prematurity (ROP)

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Abstract

Two visually monocular patients with retinopathy of prematurity, followed up for 14 and 5 years, developed progressive visual loss in their twenties and thirties, respectively. In one patient, who underwent no surgery, visual acuity deteriorated from 20/30 to 20/400 over a 14-year period. The second patient had surgery for retinal detachment. Visual acuity after surgery was 20/60. In the ensuing 2 years it dropped to counting fingers and the visual field constricted to 10 deg. We suggest that changes in the retinal pigment epithelium may compromise the photoreceptors in some ROP patients, thus leading to visual deterioration.

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Supported in part by an unrestricted grant from Research to Prevent Blindness, Inc.; presented at the American Ophthalmological Society, Hot Springs, Virginia, 24 May, 1988, and at the XVIth Meeting of the Club Jules Gonin, Bruges, 4–8 September 1988

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Tasman, W., Brown, G.C. Progressive visual loss in adults with retinopathy of prematurity (ROP). Graefe's Arch Clin Exp Ophthalmol 227, 309–311 (1989). https://doi.org/10.1007/BF02169402

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  • DOI: https://doi.org/10.1007/BF02169402

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