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Persistance de la membrane pupillaire bilatérale et forte myopie

After birth, remnants of pupillary membrane which constitute the vascular supply to the crystalline lens can persist. These are contiguous to the iris collarette causing possible deprivation amblyopia by obstructing the pupillary area. We here report the case of a 4-year-old child, born to consangui...

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Detalles Bibliográficos
Autores principales: Zerkaoui, Nouha, Laghmari, Amina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080965/
https://www.ncbi.nlm.nih.gov/pubmed/30100976
http://dx.doi.org/10.11604/pamj.2018.29.222.14297
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author Zerkaoui, Nouha
Laghmari, Amina
author_facet Zerkaoui, Nouha
Laghmari, Amina
author_sort Zerkaoui, Nouha
collection PubMed
description After birth, remnants of pupillary membrane which constitute the vascular supply to the crystalline lens can persist. These are contiguous to the iris collarette causing possible deprivation amblyopia by obstructing the pupillary area. We here report the case of a 4-year-old child, born to consanguineous parents, presenting with bilateral persistent pupillary membrane associated with high myopia. Clinical examination showed bilateral remnants of pupillary membrane, intact iris sphincter and diffuse chorioretinal atrophy in the fundus of eye . Visual acuity was difficult to assess. On the other hand, refraction test showed high myopia RE -10.75 (-3.25, 29°) LE -10 (-0.75, 180°). Treatment of bilateral persistent pupillary membrane is based on mydriatic agents, surgical excision or laser destruction. We opted for the use of mydriatic agents with total optical correction and amblyopia treatment.
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spelling pubmed-60809652018-08-10 Persistance de la membrane pupillaire bilatérale et forte myopie Zerkaoui, Nouha Laghmari, Amina Pan Afr Med J Images in Medicine After birth, remnants of pupillary membrane which constitute the vascular supply to the crystalline lens can persist. These are contiguous to the iris collarette causing possible deprivation amblyopia by obstructing the pupillary area. We here report the case of a 4-year-old child, born to consanguineous parents, presenting with bilateral persistent pupillary membrane associated with high myopia. Clinical examination showed bilateral remnants of pupillary membrane, intact iris sphincter and diffuse chorioretinal atrophy in the fundus of eye . Visual acuity was difficult to assess. On the other hand, refraction test showed high myopia RE -10.75 (-3.25, 29°) LE -10 (-0.75, 180°). Treatment of bilateral persistent pupillary membrane is based on mydriatic agents, surgical excision or laser destruction. We opted for the use of mydriatic agents with total optical correction and amblyopia treatment. The African Field Epidemiology Network 2018-04-23 /pmc/articles/PMC6080965/ /pubmed/30100976 http://dx.doi.org/10.11604/pamj.2018.29.222.14297 Text en © Nouha Zerkaoui 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 Images in Medicine
Zerkaoui, Nouha
Laghmari, Amina
Persistance de la membrane pupillaire bilatérale et forte myopie
title Persistance de la membrane pupillaire bilatérale et forte myopie
title_full Persistance de la membrane pupillaire bilatérale et forte myopie
title_fullStr Persistance de la membrane pupillaire bilatérale et forte myopie
title_full_unstemmed Persistance de la membrane pupillaire bilatérale et forte myopie
title_short Persistance de la membrane pupillaire bilatérale et forte myopie
title_sort persistance de la membrane pupillaire bilatérale et forte myopie
topic Images in Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080965/
https://www.ncbi.nlm.nih.gov/pubmed/30100976
http://dx.doi.org/10.11604/pamj.2018.29.222.14297
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