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Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes

Leber hereditary optic neuropathy (LHON) causes visual loss, predominantly in healthy young men. We recently examined a patient who previously had bilateral macular holes and subsequently developed LHON at 74 years of age. Although his central scotomas were initially attributed to the macular holes,...

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Autores principales: Shimada, Yoshiaki, Horiguchi, Masayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898147/
https://www.ncbi.nlm.nih.gov/pubmed/27335507
http://dx.doi.org/10.3109/01658107.2016.1148744
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author Shimada, Yoshiaki
Horiguchi, Masayuki
author_facet Shimada, Yoshiaki
Horiguchi, Masayuki
author_sort Shimada, Yoshiaki
collection PubMed
description Leber hereditary optic neuropathy (LHON) causes visual loss, predominantly in healthy young men. We recently examined a patient who previously had bilateral macular holes and subsequently developed LHON at 74 years of age. Although his central scotomas were initially attributed to the macular holes, his visual acuity declined following an initial improvement after operative closure of the macular holes; thus, other diagnoses, including LHON, were considered. Furthermore, macular optical coherence tomography (OCT) images remained unchanged in this time. A mitochondrial genetic analysis identified a 11778G→A mutation. From this case, we propose that LHON remains in the differential diagnosis even in older patients, as has previously been reported.
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spelling pubmed-48981472016-06-20 Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes Shimada, Yoshiaki Horiguchi, Masayuki Neuroophthalmology Case Reports Leber hereditary optic neuropathy (LHON) causes visual loss, predominantly in healthy young men. We recently examined a patient who previously had bilateral macular holes and subsequently developed LHON at 74 years of age. Although his central scotomas were initially attributed to the macular holes, his visual acuity declined following an initial improvement after operative closure of the macular holes; thus, other diagnoses, including LHON, were considered. Furthermore, macular optical coherence tomography (OCT) images remained unchanged in this time. A mitochondrial genetic analysis identified a 11778G→A mutation. From this case, we propose that LHON remains in the differential diagnosis even in older patients, as has previously been reported. Taylor & Francis 2016-03-09 /pmc/articles/PMC4898147/ /pubmed/27335507 http://dx.doi.org/10.3109/01658107.2016.1148744 Text en Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Case Reports
Shimada, Yoshiaki
Horiguchi, Masayuki
Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes
title Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes
title_full Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes
title_fullStr Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes
title_full_unstemmed Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes
title_short Leber Hereditary Optic Neuropathy Associated with Bilateral Macular Holes
title_sort leber hereditary optic neuropathy associated with bilateral macular holes
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898147/
https://www.ncbi.nlm.nih.gov/pubmed/27335507
http://dx.doi.org/10.3109/01658107.2016.1148744
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