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Imaging of Muller cell sheen dystrophy

To report a rare case of Muller cell sheen dystrophy and to describe its clinical and diagnostic aspects. A 42-year-old woman presented with unilateral defective vision. Fundus evaluation revealed bilateral glistening retinal reflexes throughout the posterior pole with a wrinkled appearance in the r...

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Autores principales: Parida, Haemoglobin, Kannan, Naresh B, Rathinam, S R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043178/
https://www.ncbi.nlm.nih.gov/pubmed/32057027
http://dx.doi.org/10.4103/ijo.IJO_930_19
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author Parida, Haemoglobin
Kannan, Naresh B
Rathinam, S R
author_facet Parida, Haemoglobin
Kannan, Naresh B
Rathinam, S R
author_sort Parida, Haemoglobin
collection PubMed
description To report a rare case of Muller cell sheen dystrophy and to describe its clinical and diagnostic aspects. A 42-year-old woman presented with unilateral defective vision. Fundus evaluation revealed bilateral glistening retinal reflexes throughout the posterior pole with a wrinkled appearance in the right. Spectral Domain-OCT in the right showed abnormal internal limiting membrane, intraretinal schisis with serous detachment at macula. Angiography revealed staining along vessels. Electroretinogram in the affected eye was negative. At 4 months of follow up, vision dropped and intraretinal schisis increased. Family screening was negative.
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spelling pubmed-70431782020-03-13 Imaging of Muller cell sheen dystrophy Parida, Haemoglobin Kannan, Naresh B Rathinam, S R Indian J Ophthalmol Case Reports To report a rare case of Muller cell sheen dystrophy and to describe its clinical and diagnostic aspects. A 42-year-old woman presented with unilateral defective vision. Fundus evaluation revealed bilateral glistening retinal reflexes throughout the posterior pole with a wrinkled appearance in the right. Spectral Domain-OCT in the right showed abnormal internal limiting membrane, intraretinal schisis with serous detachment at macula. Angiography revealed staining along vessels. Electroretinogram in the affected eye was negative. At 4 months of follow up, vision dropped and intraretinal schisis increased. Family screening was negative. Wolters Kluwer - Medknow 2020-03 2020-02-14 /pmc/articles/PMC7043178/ /pubmed/32057027 http://dx.doi.org/10.4103/ijo.IJO_930_19 Text en Copyright: © 2020 Indian Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Reports
Parida, Haemoglobin
Kannan, Naresh B
Rathinam, S R
Imaging of Muller cell sheen dystrophy
title Imaging of Muller cell sheen dystrophy
title_full Imaging of Muller cell sheen dystrophy
title_fullStr Imaging of Muller cell sheen dystrophy
title_full_unstemmed Imaging of Muller cell sheen dystrophy
title_short Imaging of Muller cell sheen dystrophy
title_sort imaging of muller cell sheen dystrophy
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7043178/
https://www.ncbi.nlm.nih.gov/pubmed/32057027
http://dx.doi.org/10.4103/ijo.IJO_930_19
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