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

Uri Rehany, Yanir Kassif, Shimon Rumelt

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

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.

Original languageEnglish
Pages (from-to)1185-1187
Number of pages3
JournalNeurology
Volume51
Issue number4
DOIs
StatePublished - Oct 1998
Externally publishedYes

Fingerprint

Dive into the research topics of 'Sneddon's syndrome: Neuro-ophthalmologic manifestations in a possible autosomal recessive pattern'. Together they form a unique fingerprint.

Cite this