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Article
October 1991

Ocular Findings Associated With a Rhodopsin Gene Codon 58 Transversion Mutation in Autosomal Dominant Retinitis Pigmentosa

Author Affiliations

From the Department of Ophthalmology, The University of Illinois at Chicago (Dr Fishman and Mr Gilbert), the Department of Ophthalmology, University of Iowa, Iowa City (Drs Stone and Sheffield), and the Department of Genetics, Trinity College, Dublin, Ireland (Dr Kenna).

Arch Ophthalmol. 1991;109(10):1387-1393. doi:10.1001/archopht.1991.01080100067044
Abstract

• Eight members of a family with autosomal dominant retinitis pigmentosa were found to have a cytosine-to-guanine (C-to-G) transversion mutation in the second nucleotide of codon 58 of the rhodopsin gene, causing a substitution of the amino acid arginine for threonine. Five of these individuals were examined clinically. There was a distinct phenotypic expression of the gene defect within this family that included a regional predilection for pigmentary changes in the inferior and inferonasal parts of the retina, as well as field impairment predominantly in the superior hemisphere. Characteristic electroretinographic recordings and psychophysical threshold profiles also helped to identify this phenotype that, on a relative basis, causes less severe photoreceptor cell functional impairment than often occurs in other subtypes of retinitis pigmentosa. This report documents the association of a clinically recognizable phenotype in a family with autosomal dominant retinitis pigmentosa and a specific gene defect at the molecular level.

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