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Duane Retraction Syndrome - EyeWiki 378 71 Duane's syndrome [1] Disease Duane retraction syndrome (also known as Stilling-Turk-Duane syndrome) is a congenital, nonprogressive strabismus syndrome originally described by Alexander Duane in 1905 [2] [3] Its characteristics include: Complete or partial (less common) absence of abduction [2] Widening of palpebral aperture with
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Duane syndrome - Wikipedia Most patients are diagnosed by the age of 10 years and Duane's is more common in girls (60 percent of the cases) than boys (40 percent of the cases) A French study reports that this syndrome accounts for 1 9% of the population of strabismic patients, 53 5% of patients are female, is unilateral in 78% of cases, and the left eye (71 9%) is
Duane retraction syndrome | About the Disease | GARD "Duane syndrome affects the ability of the eye to move from side to side Symptoms include restricted movement of eye outward and or inward and the eyeball may be pulled back into the socket In addition, the opening of the eye may be narrow Some people with Duane syndrome develop ""lazy eye"" (amblyopia), a condition that may cause vision loss in the affected eye Duane syndrome usually only
About Duane Syndrome - National Human Genome Research Institute Other names for this condition include: Duane's Retraction Syndrome (or DR syndrome), Eye Retraction Syndrome, Retraction Syndrome, Congenital retraction syndrome and Stilling-Turk-Duane Syndrome In 70 percent of DS cases, this is the only disorder the individual has However, other conditions and syndromes have been found in association with DS
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Sixth Nerve Palsies - Dizziness-and-Balance. com Duane's can resemble the much more common 6th nerve palsy, but unlike most 6ths, Duanes is congenital and also accompanied by narrowing of the eye on attempted adduction (looking inward with that eye)