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Unilateral morning glory optic disc anomaly in a case with Down syndrome

BACKGROUND: This case is unique because it is the first reported case of Down syndrome with morning glory optic disc anomaly in literature. CASE PRESENTATION: A 15-year-old girl with features of Down syndrome presented to the Clinic of Ophthalmology for a regular ophthalmologic examination. Her best...

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Autores principales: Altun, Ahmet, Altun, Gulengul, Kurna, Sevda Aydin, Olcaysu, Osman Okan, Aki, Suat Fazil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989808/
https://www.ncbi.nlm.nih.gov/pubmed/24725623
http://dx.doi.org/10.1186/1471-2415-14-48
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author Altun, Ahmet
Altun, Gulengul
Kurna, Sevda Aydin
Olcaysu, Osman Okan
Aki, Suat Fazil
author_facet Altun, Ahmet
Altun, Gulengul
Kurna, Sevda Aydin
Olcaysu, Osman Okan
Aki, Suat Fazil
author_sort Altun, Ahmet
collection PubMed
description BACKGROUND: This case is unique because it is the first reported case of Down syndrome with morning glory optic disc anomaly in literature. CASE PRESENTATION: A 15-year-old girl with features of Down syndrome presented to the Clinic of Ophthalmology for a regular ophthalmologic examination. Her best corrected visual acuity was 20/50 in the right eye and 20/20 in the left eye. The fundus examination revealed findings compatible with unilateral morning glory optic disc anomaly in the right eye. The patient underwent a complete ophthalmologic and systemic evaluation to explore possible associated findings. CONCLUSION: This case report emphasizes the importance of ophthalmic screening-examinations in Down children to rule out any vision relevant pathology.
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spelling pubmed-39898082014-04-18 Unilateral morning glory optic disc anomaly in a case with Down syndrome Altun, Ahmet Altun, Gulengul Kurna, Sevda Aydin Olcaysu, Osman Okan Aki, Suat Fazil BMC Ophthalmol Case Report BACKGROUND: This case is unique because it is the first reported case of Down syndrome with morning glory optic disc anomaly in literature. CASE PRESENTATION: A 15-year-old girl with features of Down syndrome presented to the Clinic of Ophthalmology for a regular ophthalmologic examination. Her best corrected visual acuity was 20/50 in the right eye and 20/20 in the left eye. The fundus examination revealed findings compatible with unilateral morning glory optic disc anomaly in the right eye. The patient underwent a complete ophthalmologic and systemic evaluation to explore possible associated findings. CONCLUSION: This case report emphasizes the importance of ophthalmic screening-examinations in Down children to rule out any vision relevant pathology. BioMed Central 2014-04-13 /pmc/articles/PMC3989808/ /pubmed/24725623 http://dx.doi.org/10.1186/1471-2415-14-48 Text en Copyright © 2014 Altun et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Altun, Ahmet
Altun, Gulengul
Kurna, Sevda Aydin
Olcaysu, Osman Okan
Aki, Suat Fazil
Unilateral morning glory optic disc anomaly in a case with Down syndrome
title Unilateral morning glory optic disc anomaly in a case with Down syndrome
title_full Unilateral morning glory optic disc anomaly in a case with Down syndrome
title_fullStr Unilateral morning glory optic disc anomaly in a case with Down syndrome
title_full_unstemmed Unilateral morning glory optic disc anomaly in a case with Down syndrome
title_short Unilateral morning glory optic disc anomaly in a case with Down syndrome
title_sort unilateral morning glory optic disc anomaly in a case with down syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989808/
https://www.ncbi.nlm.nih.gov/pubmed/24725623
http://dx.doi.org/10.1186/1471-2415-14-48
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