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...
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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 |
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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 |
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AT eladmoisseiev benignyellowdotmaculopathy |
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