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Occult Macular Dystrophy

Occult macular dystrophy is an inherited macular dystrophy characterized by a progressive decline of bilateral visual acuity with normal fundus appearance, fluorescein angiogram and full-field electroretinogram. This case report presents a 20-year-old female patient with bilateral progressive declin...

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Autores principales: Sayman Muslubaş, Işıl, Arf, Serra, Hocaoğlu, Mümin, Özdemir, Hakan, Karaçorlu, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082257/
https://www.ncbi.nlm.nih.gov/pubmed/27800268
http://dx.doi.org/10.4274/tjo.26234
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author Sayman Muslubaş, Işıl
Arf, Serra
Hocaoğlu, Mümin
Özdemir, Hakan
Karaçorlu, Murat
author_facet Sayman Muslubaş, Işıl
Arf, Serra
Hocaoğlu, Mümin
Özdemir, Hakan
Karaçorlu, Murat
author_sort Sayman Muslubaş, Işıl
collection PubMed
description Occult macular dystrophy is an inherited macular dystrophy characterized by a progressive decline of bilateral visual acuity with normal fundus appearance, fluorescein angiogram and full-field electroretinogram. This case report presents a 20-year-old female patient with bilateral progressive decline of visual acuity for six years. Her visual acuity was 3-4/10 in both eyes. Anterior segment and fundus examination, fluorescein angiogram and full-field electroretinogram were normal. She could read all Ishihara pseudoisochromatic plates. Fundus autofluorescence imaging was normal. There was a mild central hyporeflectance on fundus infrared reflectance imaging in both eyes. Reduced foveal thickness and alterations of the photoreceptor inner and outer segment junction were observed by optical coherence tomography in both eyes. Central scotoma was also found by microperimetry and reduced central response was revealed by multifocal electroretinogram in both eyes. These findings are consistent with the clinical characteristics of occult macular dystrophy.
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spelling pubmed-50822572016-10-31 Occult Macular Dystrophy Sayman Muslubaş, Işıl Arf, Serra Hocaoğlu, Mümin Özdemir, Hakan Karaçorlu, Murat Turk J Ophthalmol Case Report Occult macular dystrophy is an inherited macular dystrophy characterized by a progressive decline of bilateral visual acuity with normal fundus appearance, fluorescein angiogram and full-field electroretinogram. This case report presents a 20-year-old female patient with bilateral progressive decline of visual acuity for six years. Her visual acuity was 3-4/10 in both eyes. Anterior segment and fundus examination, fluorescein angiogram and full-field electroretinogram were normal. She could read all Ishihara pseudoisochromatic plates. Fundus autofluorescence imaging was normal. There was a mild central hyporeflectance on fundus infrared reflectance imaging in both eyes. Reduced foveal thickness and alterations of the photoreceptor inner and outer segment junction were observed by optical coherence tomography in both eyes. Central scotoma was also found by microperimetry and reduced central response was revealed by multifocal electroretinogram in both eyes. These findings are consistent with the clinical characteristics of occult macular dystrophy. Galenos Publishing 2016-04 2016-04-05 /pmc/articles/PMC5082257/ /pubmed/27800268 http://dx.doi.org/10.4274/tjo.26234 Text en ©Turkish Journal of Ophthalmology, Published by Galenos Publishing. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sayman Muslubaş, Işıl
Arf, Serra
Hocaoğlu, Mümin
Özdemir, Hakan
Karaçorlu, Murat
Occult Macular Dystrophy
title Occult Macular Dystrophy
title_full Occult Macular Dystrophy
title_fullStr Occult Macular Dystrophy
title_full_unstemmed Occult Macular Dystrophy
title_short Occult Macular Dystrophy
title_sort occult macular dystrophy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082257/
https://www.ncbi.nlm.nih.gov/pubmed/27800268
http://dx.doi.org/10.4274/tjo.26234
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