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Brown syndrome with severe amblyopia: a case report from Africa

Brown syndrome is a rare form of strabismus that is characterised by restriction of elevation of the eye in adduction. This is a case report of an eleven year old Nigerian girl who presented with a history of squint and poor vision. She had visual acuities of 6/24 and counting fingers in her right a...

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Autor principal: Olusanya, Bolutife Ayokunnu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449988/
https://www.ncbi.nlm.nih.gov/pubmed/26090014
http://dx.doi.org/10.11604/pamj.2015.20.56.6050
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author Olusanya, Bolutife Ayokunnu
author_facet Olusanya, Bolutife Ayokunnu
author_sort Olusanya, Bolutife Ayokunnu
collection PubMed
description Brown syndrome is a rare form of strabismus that is characterised by restriction of elevation of the eye in adduction. This is a case report of an eleven year old Nigerian girl who presented with a history of squint and poor vision. She had visual acuities of 6/24 and counting fingers in her right and left eyes respectively. There was a left hypotropia in the primary position of gaze with associated marked restriction of elevation in adduction and a positive forced duction test. Refraction revealed a refractive error of +4.50 diopters in each eye. The right visual acuity improved significantly to 6/9 with the refractive correction while the left visual acuity improved marginally to 6/60. This report demonstrates the occurrence of Brown syndrome with associated severe amblyopia in Africa. Health care providers are encouraged to promptly refer all patients, especially children, who have ocular motility disorders for early specialist intervention.
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spelling pubmed-44499882015-06-18 Brown syndrome with severe amblyopia: a case report from Africa Olusanya, Bolutife Ayokunnu Pan Afr Med J Case Report Brown syndrome is a rare form of strabismus that is characterised by restriction of elevation of the eye in adduction. This is a case report of an eleven year old Nigerian girl who presented with a history of squint and poor vision. She had visual acuities of 6/24 and counting fingers in her right and left eyes respectively. There was a left hypotropia in the primary position of gaze with associated marked restriction of elevation in adduction and a positive forced duction test. Refraction revealed a refractive error of +4.50 diopters in each eye. The right visual acuity improved significantly to 6/9 with the refractive correction while the left visual acuity improved marginally to 6/60. This report demonstrates the occurrence of Brown syndrome with associated severe amblyopia in Africa. Health care providers are encouraged to promptly refer all patients, especially children, who have ocular motility disorders for early specialist intervention. The African Field Epidemiology Network 2015-01-21 /pmc/articles/PMC4449988/ /pubmed/26090014 http://dx.doi.org/10.11604/pamj.2015.20.56.6050 Text en © Bolutife Ayokunnu Olusanya 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
Olusanya, Bolutife Ayokunnu
Brown syndrome with severe amblyopia: a case report from Africa
title Brown syndrome with severe amblyopia: a case report from Africa
title_full Brown syndrome with severe amblyopia: a case report from Africa
title_fullStr Brown syndrome with severe amblyopia: a case report from Africa
title_full_unstemmed Brown syndrome with severe amblyopia: a case report from Africa
title_short Brown syndrome with severe amblyopia: a case report from Africa
title_sort brown syndrome with severe amblyopia: a case report from africa
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449988/
https://www.ncbi.nlm.nih.gov/pubmed/26090014
http://dx.doi.org/10.11604/pamj.2015.20.56.6050
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