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Superior segmental optic hypoplasia as a differential diagnosis of glaucoma

Superior segmental optic hypoplasia (SSOH) is a congenital anomaly affecting the optic nerve head and retina. Although the conventional characterization of SSOH emphasizes the relatively superior entrance of the central retinal artery, the pallor of the superior optic disc, a superior peripapillary...

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Autor principal: Yamamoto, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557073/
https://www.ncbi.nlm.nih.gov/pubmed/31198664
http://dx.doi.org/10.4103/tjo.tjo_28_19
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author Yamamoto, Tetsuya
author_facet Yamamoto, Tetsuya
author_sort Yamamoto, Tetsuya
collection PubMed
description Superior segmental optic hypoplasia (SSOH) is a congenital anomaly affecting the optic nerve head and retina. Although the conventional characterization of SSOH emphasizes the relatively superior entrance of the central retinal artery, the pallor of the superior optic disc, a superior peripapillary halo, and thinning of the superior nerve fiber layer, we encounter many cases with rim thinning in the superior nasal region that corresponds to a nerve fiber layer defect and an inferior wedge-shaped visual field defect connecting to the blind spot. However, among Asians, such cases usually lack pallor of the superior optic disc and more resemble glaucomatous optic neuropathy. We found the prevalence of SSOH to be 0.2%/eye and 0.3%/case among Japanese. We also noted that approximately half of all SSOH eyes show visual field changes. SSOH is an important differential diagnosis of glaucoma, especially normal-tension glaucoma, in Asian populations.
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spelling pubmed-65570732019-06-13 Superior segmental optic hypoplasia as a differential diagnosis of glaucoma Yamamoto, Tetsuya Taiwan J Ophthalmol Review Article Superior segmental optic hypoplasia (SSOH) is a congenital anomaly affecting the optic nerve head and retina. Although the conventional characterization of SSOH emphasizes the relatively superior entrance of the central retinal artery, the pallor of the superior optic disc, a superior peripapillary halo, and thinning of the superior nerve fiber layer, we encounter many cases with rim thinning in the superior nasal region that corresponds to a nerve fiber layer defect and an inferior wedge-shaped visual field defect connecting to the blind spot. However, among Asians, such cases usually lack pallor of the superior optic disc and more resemble glaucomatous optic neuropathy. We found the prevalence of SSOH to be 0.2%/eye and 0.3%/case among Japanese. We also noted that approximately half of all SSOH eyes show visual field changes. SSOH is an important differential diagnosis of glaucoma, especially normal-tension glaucoma, in Asian populations. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6557073/ /pubmed/31198664 http://dx.doi.org/10.4103/tjo.tjo_28_19 Text en Copyright: © 2019 Taiwan J Ophthalmol 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 Review Article
Yamamoto, Tetsuya
Superior segmental optic hypoplasia as a differential diagnosis of glaucoma
title Superior segmental optic hypoplasia as a differential diagnosis of glaucoma
title_full Superior segmental optic hypoplasia as a differential diagnosis of glaucoma
title_fullStr Superior segmental optic hypoplasia as a differential diagnosis of glaucoma
title_full_unstemmed Superior segmental optic hypoplasia as a differential diagnosis of glaucoma
title_short Superior segmental optic hypoplasia as a differential diagnosis of glaucoma
title_sort superior segmental optic hypoplasia as a differential diagnosis of glaucoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557073/
https://www.ncbi.nlm.nih.gov/pubmed/31198664
http://dx.doi.org/10.4103/tjo.tjo_28_19
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