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Article
September 1982

Unilateral Duane's Retraction Syndrome (Type 1)

Author Affiliations

From the Neuro-ophthalmology Unit (Dr Miller) and the Eye Pathology Laboratory (Dr Green), Wilmer Ophthalmological Institute, and the Department of Pathology (Drs Kiel and Clark), The Johns Hopkins Medical Institutions, Baltimore.

Arch Ophthalmol. 1982;100(9):1468-1472. doi:10.1001/archopht.1982.01030040446016
Abstract

• Duane's retraction syndrome (DRS) is a congenital eye movement disorder characterized by abduction deficiency, adduction limitation, globe retraction, and palpebral fissure narrowing on attempted adduction. In a case of unilateral DRS, the right side of the brainstem, cavernous sinus, and orbit were completely normal. The left abducens nucleus contained no cell bodies from motor neurons, but in its rostral portion, it contained several small cell bodies believed to be compatible with internuclear neurons. The left abducens nerve was absent. The left lateral rectus muscle was partially innervated by branches from the inferior oculomotor nerve.

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