DR. SONALI SARANGI
DR. SANTOSH MAHAPATRA, DR. AYANTIKA DAS
Abstract
A very rare case was encountered when a 16yr old female came to opd with mild asthenopic symptoms with no history of nyctalopia. BCVA was 6/9,N6 both eyes with normal anterior segment. Dilated fundus examination incidentally revealed numerous diffusely scattered yellow to white polymorphous lesions extending to far periphery but sparing the macula which showed auto fluorescence. Colour vision was normal. OCT & OCTA showed the lesions to be present at the level of RPE behind the blood vessels. She was prescribed glasses and was sent for ERG & EOG. A clinical diagnosis of Benign Fleck Retinopathy was made having AR inheritance pattern. But, in our case, the patient was solely affected. Hence the report.


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