Case report of benign familial fleck retina

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...

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Bibliographic Details
Published in:TNOA Journal of Ophthalmic Science and Research 2022-01, Vol.60 (4), p.335-337
Main Authors: Bagrecha, Nipun, Prabhushanker, M, Geetha, G, Parachuri, Nikulaa
Format: Article
Language:English
Subjects:
autofluorescence
autosomal recessive
electrophysiological
fleck retina
flecked retina syndromes
inherited
optical coherence tomography
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Summary: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.
ISSN:2589-4528
2589-4536
2589-4528
DOI:10.4103/tjosr.tjosr_50_22