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Duane retraction syndrome in a patient with abnormal head position

Duane’s syndrome is a rare retraction anomaly characterized by an innervation defect in the lateral rectus muscle, limitation of abduction and adduction due to the result of abnormal innervation of the horizontal rectus muscles, changes in the eyelid fissures, and abnormal vertical eye movements. Th...

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Detalles Bibliográficos
Autores principales: Gökçe, Şule, Albayram, Zeynep Büşra, Turan, Gülizar, Biler, Elif Demirkılınç, Aydoğdu, Sema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776448/
https://www.ncbi.nlm.nih.gov/pubmed/31619934
http://dx.doi.org/10.14744/TurkPediatriArs.2018.6116
Descripción
Sumario:Duane’s syndrome is a rare retraction anomaly characterized by an innervation defect in the lateral rectus muscle, limitation of abduction and adduction due to the result of abnormal innervation of the horizontal rectus muscles, changes in the eyelid fissures, and abnormal vertical eye movements. The affected eye is displaced up and/or down in adduction. This syndrome, also known as Stilling-Turk-Duane syndrome, accounts for approximately 1 to 5% of all strabismus cases. In this article, we present a one-and-a-half-year-old male patient who had abnormal head position, and was diagnosed as having Duane retraction syndrome. Through this study, we want to draw attention to Duane retraction syndrome, which is one of the rare causes of strabismus.