unilateral sectoral retinitis pigmentosa in a patient of iranian origin

Introduction: sectoral retinitis pigmentosa (rp) is a rare clinical condition. case presentation:we present a 60-year-old female with a history of mild night blindness and decreased vision in the left eye for about 15 years. conclusions: fundus examination revealed retinal pigmentary changes in the inferotemporal sector and reduced arterial caliber. in addition, fundus autofluorescence, fluorescein angiography, multifocal electroretinogram scans and electro-oculogram confirmed these clinical findings. to the best of our knowledge, the present study is the first to describe sectorial rp in the inferotemporal sector of iranian origin.