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dc.contributor.authorRajjoub, Raneem D.
dc.contributor.authorAouchiche, Rachid
dc.date.accessioned2020-03-11T14:17:30Z
dc.date.available2020-03-11T14:17:30Z
dc.date.issued2020
dc.identifier.urihttp://hdl.handle.net/10713/12194
dc.descriptionPoster presented at the 46th annual meeting of the North American Neuro-Ophthalmology Society (NANOS), held March 7-12, 2020, in Amelia Island, Florida.en_US
dc.description.abstractTolosa-Hunt syndrome (THS) is a rare condition characterized by episodic, painful ophthalmoplegia secondary to idiopathic inflammation of the cavernous sinus, orbital apex, or superior orbital fissure, resulting in paralysis of the third, fourth, and/or sixth cranial nerves. The incidence of THS in the United States is one case per million people annually, with a mean onset of 38-41 +/- 14-16 years. Only 18 pediatric cases have been reported in the literature and there remains controversy regarding diagnostic approach and treatment strategies in children. We aim to offer an additional successful therapeutic approach.en_US
dc.language.isoen_USen_US
dc.subject.meshChilden_US
dc.subject.meshTolosa-Hunt Syndromeen_US
dc.titleA Pediatric Case of Tolosa-Hunt Syndromeen_US
dc.typePoster/Presentationen_US
dc.identifier.ispublishedNoen_US
refterms.dateFOA2020-03-11T14:17:30Z


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