Duane's retraction syndrome

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dc.authoridMutlu, Fatih Mehmet/0000-0002-7796-6511
dc.contributor.authorTomac, Suhan
dc.contributor.authorMutlu, Fatih Mehmet
dc.contributor.authorAltinsoy, Halil Ibrahim
dc.date.accessioned2024-09-18T20:04:25Z
dc.date.available2024-09-18T20:04:25Z
dc.date.issued2007
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description109th Annual Meeting of the American-Academy-of-Ophthalmology -- OCT 15-18, 2005 -- Chicago, ILen_US
dc.description.abstractPurpose: To investigate binocularity in Duane's retraction syndrome (DRS) and to evaluate whether or not there is a relationship between the sensory and clinical features of the syndrome. Methods: Clinical and sensory findings of 29 patients with DRS were recorded. Binocularity was tested with the Bagolini glasses (BG), Worth four-dot (W4D), TNO and the stereo-fly plate of the Titmus test. Results: Twenty-four (83%) patients showed fusion with the BG at near and 23 (79%) had fusion at distance. With the W4D, 23 (79%) patients had fusion at near and 19 (65%) had fusion at distance. Seven (24%) patients demonstrated normal stereoacuity, 15 (52%) had reduced stereoacuity and the remaining seven (24%) patients had no measurable stereoacuity. In patients without stereoacuity, amblyopia (p < 0.001), type 2 and 3 DRS (p = 0.031) and exotropia (p = 0.003) in primary position were more common than in those with reduced or with normal stereoacuity. Restriction of ocular ductions was also more severe in patients without stereoacuity than in those with reduced or normal stereoacuity (p = 0.019, p = 0.016). Patients with type 2 and 3 DRS were significantly more likely to have amblyopia (p = 0.037), large-angle heterotropia (p = 0.005) in primary position, upshoot or downshoot (p = 0.010) than those with type 1 DRS. Conclusions: Although approximately 75% of DRS patients had fusion and measurable stereoacuity, only 25% demonstrated normal binocularity. This report provides new data on the relationship of sensory features to most of the clinical findings of this syndrome. Sensory features, as well as most clinical features of the syndrome, are better in patients with type 1 DRS.en_US
dc.description.sponsorshipAmer Acad Ophthalmolen_US
dc.identifier.doi10.1111/j.1475-1313.2007.00517.x
dc.identifier.endpage583en_US
dc.identifier.issn0275-5408
dc.identifier.issue6en_US
dc.identifier.pmid17956363en_US
dc.identifier.scopus2-s2.0-35449004546en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage579en_US
dc.identifier.urihttps://doi.org/10.1111/j.1475-1313.2007.00517.x
dc.identifier.urihttps://hdl.handle.net/20.500.12483/8157
dc.identifier.volume27en_US
dc.identifier.wosWOS:000251089700006en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherBlackwell Publishingen_US
dc.relation.ispartofOphthalmic and Physiological Opticsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectbinocular visionen_US
dc.subjectcongenital anomaliesen_US
dc.subjectDuane's retraction syndromeen_US
dc.subjectstereopsisen_US
dc.subjectsuppressionen_US
dc.titleDuane's retraction syndromeen_US
dc.typeConference Objecten_US

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