Publication:
Extrapontine Myelinolysis in a Nine-Year Child

dc.authorscopusid7004301476
dc.authorscopusid6602646856
dc.authorscopusid7102765260
dc.authorscopusid7004140928
dc.authorscopusid7003969533
dc.contributor.authorÖztürk, F.
dc.contributor.authorGörk, S.
dc.contributor.authorAydin, Mahmut
dc.contributor.authorIncesu, L.
dc.contributor.authorBaysal, K.
dc.date.accessioned2020-06-21T15:53:03Z
dc.date.available2020-06-21T15:53:03Z
dc.date.issued1998
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Öztürk] Fadil, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Görk] Semih, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aydin] Murat, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Incesu] Lütfi, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Radiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Baysal] Kemal, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Pediatrics, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractExtrapontine myelinolysis in the pediatric age group is very rare. We report a nine-year-old girl with the classical clinical syndrome of pontine and extrapontine myelinolysis following liver trauma due to a traffic accident. She was referred to our hospital for further investigation of convulsions due to severe postoperative hyponatremia. She had no hypoxic event or other identifiable cause for the neurological symptoms. Neurological deterioration began about two days after correction of hyponatremia and followed a period of temporary improvement in hyponatremic encephalopathy. Diagnosis of extrapontine myelinolysis was confirmed with the identification of typical features on magnetic resonance imaging. The rapid correction of hyponatremia seemed the most likely cause since other biochemical tests including liver function tests were all within normal ranges. The long term clinical outcome was good. It is important to carefully monitor the rate of correction in electrolyte disturbances, and to consider the individual variation in response to therapy.en_US
dc.identifier.endpage584en_US
dc.identifier.issn0041-4301
dc.identifier.issn2791-6421
dc.identifier.issue4en_US
dc.identifier.pmid10028868
dc.identifier.scopus2-s2.0-0032177218
dc.identifier.scopusqualityQ3
dc.identifier.startpage579en_US
dc.identifier.volume40en_US
dc.identifier.wosWOS:000077582800014
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherTurkish Journal of Pediatricsen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.relation.journalTurkish Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChilden_US
dc.subjectExtrapontine Myelinolysisen_US
dc.subjectHyponatremiaen_US
dc.titleExtrapontine Myelinolysis in a Nine-Year Childen_US
dc.typeArticleen_US
dspace.entity.typePublication

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