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  Vol. 72 No. 2, August 1964 TABLE OF CONTENTS
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Duane's Syndrome: A Brain Stem Lesion

An Electromyographic Study

FREDERICK C. BLODI, MD; M. W. VAN ALLEN, MD; J. C. YARBROUGH, MD

Arch Ophthalmol. 1964;72(2):171-177.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Duane's syndrome consists of a reduction in or loss of abduction of the globe, retraction on adduction with occasional limitation of this movement, a narrowing of the palpebral fissure on adduction, and widening of the fissure on attempted abduction. There is a deficiency of convergence and occasionally an up or down deviation on adduction. The syndrome is congenital and cases of familial incidence have been reported. Numerous theories have been brought forward to explain these unusual anomalies of ocular motility. Most of the older hypotheses attributed this abnormality to pathologic changes in the extraocular muscles or in their tendons.1,2

Many found the external rectus muscle transformed into a band of rather inelastic cord-like tissue.3 This could explain the retraction on adduction but cannot account for the narrowing of the palpebral fissure. Such a band should also eventually lead to a secondary strabismus which is usually absent in this . . . [Full Text PDF of this Article]


Author Affiliations

Iowa City, Iowa; Anderson, SC

From the Neurosensory Center of the Department of Neurology and Ophthalmology, College of Medicine, State University of Iowa. The Neurosensory Center is supported by Program-Project grant B-3354 of the National Institute of Neurological Diseases and Blindness, publication No. 29.


Footnotes

Presented at the annual meeting of the American Academy of Ophthalmology and Otolaryngology, New York, Oct 22, 1963.

Supported in part by the Harriett Ames Charitable Trust Grant in Cerebral Palsy awarded by the United Cerebral Palsy Research and Educational Foundation.



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