Results 141 to 150 of about 1,604 (176)
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Sensory adaptations in Duane's retraction syndrome

Acta Ophthalmologica Scandinavica, 1995
ABSTRACT Knowledge of the sensory status of patients with Duane's retraction syndrome is limited. Fourteen patients with type A Duane's retraction syndrome, aged 6 to 22 years, were assessed prospectively and their sensory findings and the nature of their sensory symptoms detailed.
H P, Orton, J P, Burke
openaire   +2 more sources

Duane retraction syndrome mimicking orbital fracture

British Journal of Oral and Maxillofacial Surgery, 2011
We describe the case of a 20-year-old patient who presented at the accident and emergency department with symptoms and signs of fractures of the zygomatic complex and orbit following an assault. He was later discovered to have Duane retraction syndrome, a rare congenital disorder of eye movement that has some of the clinical characteristics of ...
Simon, Toledano   +2 more
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Duane's retraction syndrome.

Journal of the American Optometric Association, 1992
The clinical findings for 29 patients with Duane's retraction syndrome (DRS) are reported. Similar to other studies, a preponderance of females, left eye involvement, and type I DRS occurred. The incidence of both anisometropia and amblyopia was somewhat higher than for the normal population.
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Pseudo-Duane's retraction syndrome.

Transactions of the American Ophthalmological Society, 1977
Five patients presented with signs that were similar to but opposite from Duane's retraction syndrome. Most had a history of orbital trauma. On attempted abduction a narrowing of the palpebral fissure and retraction of the globe was observed. Diplopia with lateral gaze was present. Roentgenograms (polytomograms) showed involvement of the medial orbital
T D, Duane, N J, Schatz, A R, Caputo
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Acquired Duane's Retraction Syndrome

Journal of Pediatric Ophthalmology & Strabismus, 1996
A, Akman   +3 more
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Familial Duane's retraction syndrome.

Journal of the American Optometric Association, 1999
Duane's retraction syndrome (DRS) has been described as a clinical entity for more than a century. Although the majority of cases occur spontaneously, some cases of DRS are inherited.A young Romanian boy with a known left abduction deficit was determined to have DRS.
N L, Busch   +3 more
openaire   +1 more source

Duane's Retraction Syndrome - Plus

Journal of Pediatric Ophthalmology & Strabismus, 1982
E R, O'Malley   +2 more
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Duane's Retraction Syndrome

American Journal of Ophthalmology, 1961
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