Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5705386 | Ophthalmology | 2017 | 10 Pages |
Abstract
A new retinal phenotype is described, which is characterized by bilateral multiple early-onset yellow dots at the macula. Visual function is normal, and the condition is nonprogressive. In familial cases, the phenotype seems to be inherited in an autosomal dominant manner, but a causative gene is yet to be ascertained.
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Authors
Arundhati MD(Res), FRCOphth, Aleksandra MD, Martina MD, Robert A. MD, FACS, Zubair M. PhD, Graham E. PhD, Valentina PhD, Gavin PhD, Andrew R. MD(Res), FRCOphth, Robert B. MD, PhD, Audina MD, Anthony T. FRCOphth, FMedSci,