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Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc
Fovea plana is a congenital condition characterized by anatomic absence of the foveal pit. It may be isolated or associated with congenital ocular anomalies. In this report, we present a case of fovea plana associated with situs inversus of the optic disc, optic disc hypoplasia, tilted optic disc, a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338751/ https://www.ncbi.nlm.nih.gov/pubmed/32631023 http://dx.doi.org/10.4274/tjo.galenos..2020.98415 |
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author | Şekeryapan Gediz, Berrak Şekeroğlu, Mehmet Ali |
author_facet | Şekeryapan Gediz, Berrak Şekeroğlu, Mehmet Ali |
author_sort | Şekeryapan Gediz, Berrak |
collection | PubMed |
description | Fovea plana is a congenital condition characterized by anatomic absence of the foveal pit. It may be isolated or associated with congenital ocular anomalies. In this report, we present a case of fovea plana associated with situs inversus of the optic disc, optic disc hypoplasia, tilted optic disc, and prepapillary vascular loop and with best corrected visual acuity of 20/32. The aim of this report is to demonstrate the coexistence of very rare multiple optic disc anomalies and fovea plana, and also to emphasize that the use of multimodal imaging methods facilitates the identification of rare anomalies. |
format | Online Article Text |
id | pubmed-7338751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-73387512020-07-14 Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc Şekeryapan Gediz, Berrak Şekeroğlu, Mehmet Ali Turk J Ophthalmol Case Report Fovea plana is a congenital condition characterized by anatomic absence of the foveal pit. It may be isolated or associated with congenital ocular anomalies. In this report, we present a case of fovea plana associated with situs inversus of the optic disc, optic disc hypoplasia, tilted optic disc, and prepapillary vascular loop and with best corrected visual acuity of 20/32. The aim of this report is to demonstrate the coexistence of very rare multiple optic disc anomalies and fovea plana, and also to emphasize that the use of multimodal imaging methods facilitates the identification of rare anomalies. Galenos Publishing 2020-06 2020-06-27 /pmc/articles/PMC7338751/ /pubmed/32631023 http://dx.doi.org/10.4274/tjo.galenos..2020.98415 Text en © Copyright 2020 by Turkish Ophthalmological Association | Turkish Journal of Ophthalmology, published by Galenos Publishing House. 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 Şekeryapan Gediz, Berrak Şekeroğlu, Mehmet Ali Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc |
title | Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc |
title_full | Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc |
title_fullStr | Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc |
title_full_unstemmed | Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc |
title_short | Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc |
title_sort | multimodal imaging in a case of fovea plana associated with situs inversus of the optic disc |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338751/ https://www.ncbi.nlm.nih.gov/pubmed/32631023 http://dx.doi.org/10.4274/tjo.galenos..2020.98415 |
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