Benign yellow dot maculopathy

Purpose: To describe a new family with benign yellow dot maculopathy. Observations: A young male patient was found to have bilateral multiple small yellow dots in both maculae. Visual acuity and color vision were normal, and no pathological findings were demonstrated on automated visual field, optic...

Full description

Bibliographic Details
Main Author: Elad Moisseiev
Format: Article
Language:English
Published: Elsevier 2018-06-01
Series:American Journal of Ophthalmology Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2451993617302487
id doaj-7abf97e43da84f799dacb4b2d8559dc5
record_format Article
spelling doaj-7abf97e43da84f799dacb4b2d8559dc52020-11-24T21:04:02ZengElsevierAmerican Journal of Ophthalmology Case Reports2451-99362018-06-01101315Benign yellow dot maculopathyElad Moisseiev0Department of Ophthalmology, Tel Aviv Medical Center, Tel Aviv, Israel; Affiliated to the Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Department of Ophthalmology, Tel Aviv Medical Center, Weitzman 6 St., Tel Aviv, 64239, Israel.Purpose: To describe a new family with benign yellow dot maculopathy. Observations: A young male patient was found to have bilateral multiple small yellow dots in both maculae. Visual acuity and color vision were normal, and no pathological findings were demonstrated on automated visual field, optical coherence tomography (OCT) and electrophysiological testing. Examination of his parents revealed similar findings in his mother, suggesting autosomal dominant inheritance. No deterioration of vision occurred over long term follow up. These findings are consistent with the newly described phenotype of benign yellow dot maculopathy. Conclusions and importance: This is the first report of patients with benign yellow dot maculopathy since its original description, and the first to document it in a family of North African descent. This report will serve to raise awareness to this phenotype, which may be more common than currently known. Keywords: Yellow dot, Maculopathy, Phenotype, Familialhttp://www.sciencedirect.com/science/article/pii/S2451993617302487
collection DOAJ
language English
format Article
sources DOAJ
author Elad Moisseiev
spellingShingle Elad Moisseiev
Benign yellow dot maculopathy
American Journal of Ophthalmology Case Reports
author_facet Elad Moisseiev
author_sort Elad Moisseiev
title Benign yellow dot maculopathy
title_short Benign yellow dot maculopathy
title_full Benign yellow dot maculopathy
title_fullStr Benign yellow dot maculopathy
title_full_unstemmed Benign yellow dot maculopathy
title_sort benign yellow dot maculopathy
publisher Elsevier
series American Journal of Ophthalmology Case Reports
issn 2451-9936
publishDate 2018-06-01
description Purpose: To describe a new family with benign yellow dot maculopathy. Observations: A young male patient was found to have bilateral multiple small yellow dots in both maculae. Visual acuity and color vision were normal, and no pathological findings were demonstrated on automated visual field, optical coherence tomography (OCT) and electrophysiological testing. Examination of his parents revealed similar findings in his mother, suggesting autosomal dominant inheritance. No deterioration of vision occurred over long term follow up. These findings are consistent with the newly described phenotype of benign yellow dot maculopathy. Conclusions and importance: This is the first report of patients with benign yellow dot maculopathy since its original description, and the first to document it in a family of North African descent. This report will serve to raise awareness to this phenotype, which may be more common than currently known. Keywords: Yellow dot, Maculopathy, Phenotype, Familial
url http://www.sciencedirect.com/science/article/pii/S2451993617302487
work_keys_str_mv AT eladmoisseiev benignyellowdotmaculopathy
_version_ 1716772314660470784