Miller Fisher syndrome

dc.contributor.authorAkinci, G
dc.contributor.authorPolat, M
dc.contributor.authorTosun, A
dc.contributor.authorSerdaroglu, G
dc.contributor.authorGökben, S
dc.contributor.authorTekgül, H
dc.date.accessioned2025-04-10T10:32:57Z
dc.date.available2025-04-10T10:32:57Z
dc.description.abstractMiller Fisher syndrome is characterized by the acute onset of ophthalmoplegia, ataxia, and areflexia. Anti-GQ1b antibodies are useful markers for the differential diagnosis of Miller Fisher syndrome. We describe the case of a seven-year-old male who presented with a four-day history of diplopia and ophthalmoplegia following a febrile flu-like illness with sore throat. On examination he was found to have ataxia, areflexia and ophthalmoplegia, and a diagnosis of Miller Fisher syndrome was made after the exclusion of other conditions and concomitant with electrophysiological findings on electromyography. Although this disorder has a rare incidence, it should still be considered in the differential diagnosis in our country.
dc.identifier.issn0041-4301
dc.identifier.urihttp://hdl.handle.net/20.500.14701/39261
dc.language.isoEnglish
dc.titleMiller Fisher syndrome
dc.typeArticle

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