Bilateral type III Duane syndrome: a case report.

Autor:	García E; Servicio de Oftalmología, Hospital Universitario de Guadalajara, Guadalajara - Spain., Fernández De Arévalo BT; Servicio de Oftalmología, Hospital Universitario de Guadalajara, Guadalajara - Spain., Arévalo EM; Servicio de Oftalmología, Hospital Universitario de Guadalajara, Guadalajara - Spain., Mhanna H; Servicio de Oftalmología, Hospital Universitario de Guadalajara, Guadalajara - Spain., Alija M; Servicio de Oftalmología, Hospital Universitario de Guadalajara, Guadalajara - Spain.
Jazyk:	angličtina
Zdroj:	European journal of ophthalmology [Eur J Ophthalmol] 2015 Dec 01; Vol. 26 (1), pp. e1-3. Date of Electronic Publication: 2015 Dec 01.
DOI:	10.5301/ejo.5000659
Abstrakt:	Purpose: Duane syndrome (DS) belongs to a group of congenital retraction syndromes, the incidence of which varies between 2% and 4% in patients with strabismus. In most cases the damage is unilateral, but it manifests as bilateral in about 20% of cases. According to the classification of Huber, type III DS exhibits a limitation of abduction and adduction. Methods: We report the case of a 5-year-old boy from Eastern Europe who was taken to the hospital because he was unable to move both eyes horizontally from birth and had not been previously seen by an ophthalmologist. Results: The examination showed inability to abduct and adduct bilaterally, with narrowing of the palpebral fissures on attempted adduction. The patient was diagnosed with bilateral type III DS. Conclusions: Treatment is individualized on a case-by-case basis. For our patient, monitoring by way of regular checkups was chosen, with the parents rejecting surgery for now.
Databáze:	MEDLINE
Externí odkaz:	Zobrazit plný text záznamu