Hyperpyrexia Associated with Congenital Long QT Syndrome

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dc.contributor.authorTarakci, Nuriye
dc.contributor.authorKonak, Murat
dc.contributor.authorAltunhan, Huseyin
dc.contributor.authorAlp, Hayrullah
dc.contributor.authorOrs, Rahmi
dc.date.accessioned2024-02-23T14:45:53Z
dc.date.available2024-02-23T14:45:53Z
dc.date.issued2014
dc.departmentNEÜen_US
dc.description.abstractCongenital long QT syndrome (CLQTS) is a genetic disorder presented with prolonged QT interval. In these patients, risk of sudden cardiac death due to ventricular tachyarrhythmias is high. Bradycardia may exhibit as a result of intrauterine fetal atrioventricular block, sinus bradycardia, tachycardia in these patient. Prolonged QT interval and multisystem involvement such as sensorineural hearing loss, muscle paralysis, immune deficiency, syndactyly have been reported in these patient. We have detected hyperpyrexia without clinical immunodeficiency and infection in our patient. To our knowledge, our patient is the first case in the literatureen_US
dc.identifier.endpage913en_US
dc.identifier.issn2602-3032
dc.identifier.issn2602-3040
dc.identifier.issue4en_US
dc.identifier.startpage909en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12452/17662
dc.identifier.volume39en_US
dc.identifier.wosWOS:000216471400034en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isotren_US
dc.publisherCukurova Univ, Fac Medicineen_US
dc.relation.ispartofCukurova Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCongenital Long Qt Syndromeen_US
dc.subjectHyperpyrexiaen_US
dc.titleHyperpyrexia Associated with Congenital Long QT Syndromeen_US
dc.typeArticleen_US

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