| BRIEF COMMUNICATION |
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| Year : 2022 | Volume
: 60
| Issue : 4 | Page : 335-337 |
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Case report of benign familial fleck retina
Nipun Bagrecha, M Prabhushanker, G Geetha, Nikulaa Parachuri
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
India
 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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