Unilateral retinitis pigmentosa sine pigmento
a case report
DOI:
https://doi.org/10.70313/2718.7446.v17.n03.353Keywords:
retinitis pigmentosa, sine pigmentum, unilateralAbstract
Our objective is to present a case of unilateral retinitis pigmentosa (RP) sine pigmento, a 41-year-old female patient evaluated at our institution with a 2-year evolution of decreased visual acuity in the right eye (RE). On physical examination, visual acuity in right eye 7/10 best corrected and in left eye 10/10 without correction. Biomicroscopy in the right eye showed a posterior stellate subcapsular cataract and fundus examination revealed arteriolar narrowing, alteration of the retinal pigment epithelium and whitish lesions in the macular region, which were also found in the retinal periphery. The computed visual field of the RE showed a contraction pattern, while the electroretinogram indicated a subnormal response under scotopic conditions in the RE. On the other hand, studies performed in the LE were found to be within normal parameters. In conclusion, the presentation of a case of unilateral retinitis pigmentosa sine pigmento is extremely unusual, which motivated us to study this case in depth.
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