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Year : 2022  |  Volume : 60  |  Issue : 4  |  Page : 335-337

Case report of benign familial fleck retina

Department of Vitreo-Retina, Sankara Eye Hospital, Sathy Road, Sivanandapuram, Coimbatore, Tamil Nadu, India

Correspondence Address:
Nipun Bagrecha
Sankara Eye Hospital, Sathy Road, Sivanandapuram, Coimbatore - 641 035, Tamil Nadu
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/tjosr.tjosr_50_22

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Benign familial fleck Retina is a rare inherited retinal disease first reported by Sabel Aish and Dajani in 1980. It is an autosomal recessive condition associated with a distinctive retinal appearance with no apparent visual or electrophysiological deficits. Fundus photography, autofluorescence and enhanced depth optical coherence tomography B-scan imaging modalities aid in the diagnosis. We present a case report of a 19-year-old female diagnosed with benign familial fleck retina which belongs to a heterogeneous group of flecked retina syndromes, and should be considered in patients with yellowish-white retinal lesions sparing the macula.

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