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Colobome maculaire unilatérale: à propos d’un cas
Macular coloboma is a congenital condition characterized by failure of closure of the fetal intraocular fissure which may have a hereditary origin. Clinically, it is characterized by decreased visual acuity with macular excavated lesion characterized by missing or rudimentary retinal tissue and scle...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697988/ https://www.ncbi.nlm.nih.gov/pubmed/29184607 http://dx.doi.org/10.11604/pamj.2017.28.55.12744 |
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author | El Bahloul, Meriem Chraïbi, Fouad Mohammed, Marrakchi Abdellaoui, Meriem Benatiya, Idriss |
author_facet | El Bahloul, Meriem Chraïbi, Fouad Mohammed, Marrakchi Abdellaoui, Meriem Benatiya, Idriss |
author_sort | El Bahloul, Meriem |
collection | PubMed |
description | Macular coloboma is a congenital condition characterized by failure of closure of the fetal intraocular fissure which may have a hereditary origin. Clinically, it is characterized by decreased visual acuity with macular excavated lesion characterized by missing or rudimentary retinal tissue and scleral ectasia. Macular OCT strongly supports the diagnosis and electrophysiology examination, if requested, is altered. Differential diagnosis includes pathologies causing atrophic and excavated macular lesion, in particular congenital toxoplasmosis. |
format | Online Article Text |
id | pubmed-5697988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-56979882017-11-28 Colobome maculaire unilatérale: à propos d’un cas El Bahloul, Meriem Chraïbi, Fouad Mohammed, Marrakchi Abdellaoui, Meriem Benatiya, Idriss Pan Afr Med J Case Report Macular coloboma is a congenital condition characterized by failure of closure of the fetal intraocular fissure which may have a hereditary origin. Clinically, it is characterized by decreased visual acuity with macular excavated lesion characterized by missing or rudimentary retinal tissue and scleral ectasia. Macular OCT strongly supports the diagnosis and electrophysiology examination, if requested, is altered. Differential diagnosis includes pathologies causing atrophic and excavated macular lesion, in particular congenital toxoplasmosis. The African Field Epidemiology Network 2017-09-21 /pmc/articles/PMC5697988/ /pubmed/29184607 http://dx.doi.org/10.11604/pamj.2017.28.55.12744 Text en © Meriem El Bahloul et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. 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 El Bahloul, Meriem Chraïbi, Fouad Mohammed, Marrakchi Abdellaoui, Meriem Benatiya, Idriss Colobome maculaire unilatérale: à propos d’un cas |
title | Colobome maculaire unilatérale: à propos d’un cas |
title_full | Colobome maculaire unilatérale: à propos d’un cas |
title_fullStr | Colobome maculaire unilatérale: à propos d’un cas |
title_full_unstemmed | Colobome maculaire unilatérale: à propos d’un cas |
title_short | Colobome maculaire unilatérale: à propos d’un cas |
title_sort | colobome maculaire unilatérale: à propos d’un cas |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697988/ https://www.ncbi.nlm.nih.gov/pubmed/29184607 http://dx.doi.org/10.11604/pamj.2017.28.55.12744 |
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