Results 111 to 120 of about 797 (155)
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DUANE RETRACTION SYNDROME

Ophthalmology Clinics of North America, 2001
Duane retraction syndrome (DRS) consists of deficient horizontal eye movements, eyelid retraction, palpebral fissure narrowing, and abnormal vertical eye movements. Most cases are sporadic and unilateral (usually left side) with a slight female predominance. Several associated ocular and systemic conditions have been described in DRS patients.
G, Alexandrakis, R A, Saunders
openaire   +2 more sources

Management of Duane Retraction Syndrome

Journal of Pediatric Ophthalmology & Strabismus, 2005
Background: Duane retraction syndrome is the most common cause of congenital aberrant ocular innervation. We report referral practices, clinical characteristics and complications, prevalence of congenital and familial anomalies, and management outcomes from a clinic-based series. Methods:
Brian, Chua   +3 more
openaire   +2 more sources

Vertical Duane's Retraction Syndrome

American Journal of Ophthalmology, 1996
We report three patients with a rare variant of Duane's retraction syndrome.Eye movements were recorded by electro-oculography. One patient underwent electro-myography.All patients showed V-incommitance and twitch abduction on vertical saccades. Electromyography showed lateral rectus muscle firing activity during upgaze and downgaze.Our patients showed
Weinacht S, Huber A, Gottlob I
openaire   +3 more sources

Duane Retraction Syndrome on the Arabian Peninsula

Strabismus, 2007
To describe the clinical features of patients from the Arabian Peninsula with Duane retraction syndrome (DRS).Retrospective chart review of patients referred to the King Khaled Eye Specialist Hospital in Riyadh, Saudi Arabia from 1982 to 2003 with a diagnosis of DRS.
Arif O Khan, Darren T Oystreck
exaly   +3 more sources

Duane's Retraction Syndrome

Archives of Ophthalmology, 1982
To the Editor. —I read with great interest the article entitled "Central Ocular Motor Abnormalities in Duane's Retraction Syndrome" by Gourdeau et al in theArchives(1981;99:1809-1810). These authors suggest that Duane's retraction syndrome is produced by a primary brainstem abnormality involving premotor structures.
openaire   +2 more sources

Refractive Profile in Duane Retraction Syndrome

Nigerian Journal of Ophthalmology, 2022
Aim: To study the refractive error profile of patients with Duane retraction syndrome (DRS). Methods: We conducted a retrospective analysis of patients diagnosed with DRS between January 2015 and December 2018 at a tertiary eye center.
Raveendra Murthy, Sowmya, Gupta, Kanika
openaire   +2 more sources

Duane's Retraction Syndrome

Australasian journal of optometry, The, 1985
ABSTRACT: The condition of Duane's retraction syndrome is reviewed, and data presented from 5 cases.
P.G. Swann, K.D. Cameron
exaly   +2 more sources

Transposition procedures in Duane retraction syndrome

Journal of American Association for Pediatric Ophthalmology and Strabismus, 2019
Duane retraction syndrome, or Duane syndrome (DS), is one of several congenital cranial dysinnervation disorders. Patients present with limited horizontal eye movement(s) and globe retraction with eyelid fissure narrowing on attempted adduction due to co-contraction of the lateral and medial rectus muscles in one or both eyes.
Jefferson J, Doyle, David G, Hunter
openaire   +2 more sources

Up- and Downshoot in Duane's Retraction Syndrome

Journal of Pediatric Ophthalmology & Strabismus, 1986
ABSTRACT Up- and downshoot of the adducted eye in patients with Duane's retraction syndrome was surgically eliminated in five patients by posterior fixation of the horizontal rectus muscles. Retroequatorial fixation of these muscles reduces sideslip and thus a vertical effect of the co-contracting horizontal rectus muscles.
G K, von Noorden, E, Murray
openaire   +3 more sources

Bilateral familial Duane’s retraction syndrome

Optometry - Journal of the American Optometric Association, 2007
Duane's retraction syndrome (DRS) is a congenital oculomotor anomaly that is accompany by globe retraction with simultaneous narrowing of the palpebral fissure on attempted adduction. Hereditary factors have been postulated to be associated with the development of DRS since 1879.
Lily Y, Zhu-Tam, Andrew S, Gurwood
openaire   +2 more sources

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