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Multiple Ocular and Systemic Disorders in Association with Bilateral Duane's Retraction Syndrome

Duane's retraction syndrome (DRS) is characterized by limitations in horizontal eye movements, globe retraction, and palpebral fissure narrowing on attempted adduction. This disorder is caused by a disturbance in innervation originating in the brain stem and represents <1% of all cases of st...

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Autores principales: Zare, Mohammad Ali, Akbari, Mohammad Reza, Kiarudi, Mohammad Yaser, Mehrjardi, Hadi Zare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968148/
https://www.ncbi.nlm.nih.gov/pubmed/27555711
http://dx.doi.org/10.4103/0974-9233.186119
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author Zare, Mohammad Ali
Akbari, Mohammad Reza
Kiarudi, Mohammad Yaser
Mehrjardi, Hadi Zare
author_facet Zare, Mohammad Ali
Akbari, Mohammad Reza
Kiarudi, Mohammad Yaser
Mehrjardi, Hadi Zare
author_sort Zare, Mohammad Ali
collection PubMed
description Duane's retraction syndrome (DRS) is characterized by limitations in horizontal eye movements, globe retraction, and palpebral fissure narrowing on attempted adduction. This disorder is caused by a disturbance in innervation originating in the brain stem and represents <1% of all cases of strabismus. It is postulated that this syndrome is due to an insult during the early weeks (8–10 weeks) of pregnancy and is 10–20 times more frequently associated with other systemic congenital anomalies. This case report of bilateral DRS included bilateral iris-retinal coloboma and congenital heart disease, sensory hearing loss, and inguinal hernia.
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spelling pubmed-49681482016-08-23 Multiple Ocular and Systemic Disorders in Association with Bilateral Duane's Retraction Syndrome Zare, Mohammad Ali Akbari, Mohammad Reza Kiarudi, Mohammad Yaser Mehrjardi, Hadi Zare Middle East Afr J Ophthalmol Case Report Duane's retraction syndrome (DRS) is characterized by limitations in horizontal eye movements, globe retraction, and palpebral fissure narrowing on attempted adduction. This disorder is caused by a disturbance in innervation originating in the brain stem and represents <1% of all cases of strabismus. It is postulated that this syndrome is due to an insult during the early weeks (8–10 weeks) of pregnancy and is 10–20 times more frequently associated with other systemic congenital anomalies. This case report of bilateral DRS included bilateral iris-retinal coloboma and congenital heart disease, sensory hearing loss, and inguinal hernia. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4968148/ /pubmed/27555711 http://dx.doi.org/10.4103/0974-9233.186119 Text en Copyright: © Middle East African Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Zare, Mohammad Ali
Akbari, Mohammad Reza
Kiarudi, Mohammad Yaser
Mehrjardi, Hadi Zare
Multiple Ocular and Systemic Disorders in Association with Bilateral Duane's Retraction Syndrome
title Multiple Ocular and Systemic Disorders in Association with Bilateral Duane's Retraction Syndrome
title_full Multiple Ocular and Systemic Disorders in Association with Bilateral Duane's Retraction Syndrome
title_fullStr Multiple Ocular and Systemic Disorders in Association with Bilateral Duane's Retraction Syndrome
title_full_unstemmed Multiple Ocular and Systemic Disorders in Association with Bilateral Duane's Retraction Syndrome
title_short Multiple Ocular and Systemic Disorders in Association with Bilateral Duane's Retraction Syndrome
title_sort multiple ocular and systemic disorders in association with bilateral duane's retraction syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968148/
https://www.ncbi.nlm.nih.gov/pubmed/27555711
http://dx.doi.org/10.4103/0974-9233.186119
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