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Sneddon's syndrome: neuro-ophthalmologic manifestations in a possible autosomal recessive pattern.

作者信息

Rehany U, Kassif Y, Rumelt S

机构信息

Department of Ophthalmology, Western Galilee-Nahariya Medical Center, Nahariya, Israel.

出版信息

Neurology. 1998 Oct;51(4):1185-7. doi: 10.1212/wnl.51.4.1185.

Abstract

Sneddon's syndrome is a rare neurodermatologic disorder that is manifested by multiple cerebrovascular accidents and livedo reticularis. The authors describe two siblings from one family with Sneddon's syndrome, suggesting autosomal recessive inheritance. The propositus presented with internuclear ophthalmoplegia and ophthalmic artery occlusion. These manifestations as well as the autosomal recessive inheritance have not yet been reported in Sneddon's syndrome.

摘要

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