Results 171 to 180 of about 13,573 (219)
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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
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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
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Archives of Ophthalmology, 1972
Medial rectus innervation was always normal, and lateral rectus innervation was always abnormal. Lateral rectus overactivity accompanied deficient adduction. Lateral rectus underactivity accompanied abduction deficiency and was reflected in slowed saccadic abduction movements.
A B, Scott, G Y, Wong
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Medial rectus innervation was always normal, and lateral rectus innervation was always abnormal. Lateral rectus overactivity accompanied deficient adduction. Lateral rectus underactivity accompanied abduction deficiency and was reflected in slowed saccadic abduction movements.
A B, Scott, G Y, Wong
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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.
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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.
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Vertical Duane's Retraction Syndrome
American Journal of Ophthalmology, 1996We 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
S, Weinacht, A, Huber, I, Gottlob
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Clinical and Experimental Optometry, 1985
ABSTRACT: The condition of Duane's retraction syndrome is reviewed, and data presented from 5 cases.
P.G. Swann, K.D. Cameron
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ABSTRACT: The condition of Duane's retraction syndrome is reviewed, and data presented from 5 cases.
P.G. Swann, K.D. Cameron
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2016
Duane retraction syndrome is a unilateral or bilateral condition characterized by abnormal innervation to the extraocular muscles that results in limitation of eye movement and co-contraction of muscles that are normally antagonists (Duane, Arch Ophthalmol 34:133–59, 1905).
Ashley Abraham +2 more
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Duane retraction syndrome is a unilateral or bilateral condition characterized by abnormal innervation to the extraocular muscles that results in limitation of eye movement and co-contraction of muscles that are normally antagonists (Duane, Arch Ophthalmol 34:133–59, 1905).
Ashley Abraham +2 more
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Acquired Duane's Retraction Syndrome
Journal of Pediatric Ophthalmology & Strabismus, 1996A, Akman +3 more
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Journal of the American Optometric Association, 1990
Duane's retraction syndrome (DRS) is a congenital abnormality of ocular motility that occurs in about 1% of strabismic patients. Three types have been described and the clinical features include incomitant horizontal strabismus, restricted motility and globe retraction.
D E, Harmon, S A, Primo
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Duane's retraction syndrome (DRS) is a congenital abnormality of ocular motility that occurs in about 1% of strabismic patients. Three types have been described and the clinical features include incomitant horizontal strabismus, restricted motility and globe retraction.
D E, Harmon, S A, Primo
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