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dc.contributor.authorBademci G.
dc.contributor.authorEvliyaoglu C.
dc.contributor.authorKeskil S.
dc.date.accessioned2020-06-25T15:13:34Z
dc.date.available2020-06-25T15:13:34Z
dc.date.issued2005
dc.identifier.issn00223085
dc.identifier.urihttps://hdl.handle.net/20.500.12587/1853
dc.descriptionPubMed: 16206741en_US
dc.description.abstractIn Type I split cord malformation (SCM) lesions, the osteocartilaginous spur and its dural sleeve are almost always located in the caudal extent of the median cleft. The authors present a case of lumbar myelomeningocele associated with a thoracic Type I SCM in which an osseous septum is uniquely situated in the proximal extent of the median cleft. Split cord malformations are cord-tethering lesions, which may be associated with a myelomeningocele that causes additional tethering, even in the opposite direction; therefore, both lesions should be treated. In view of this unique case, however, the surgical approach used for tethering lesions in such cases of complex spina bifida should perhaps be tailored. Whenever feasible, meticulous preoperative examination of a patient with spina bifida, including entire craniospinal magnetic resonance imaging followed with perioperative dynamic evaluation, is important for the effectiveness and safety of the surgery.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDiastematomyeliaen_US
dc.subjectMadian cleften_US
dc.subjectPediatric neurosurgeryen_US
dc.subjectSplit cord malformationen_US
dc.subjectTethered corden_US
dc.titleProximally situated osseous septum in complex spina bifida: Case reporten_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume102 PEDIATRICSen_US
dc.identifier.issueSUPPL. 1en_US
dc.identifier.startpage92en_US
dc.identifier.endpage95en_US
dc.relation.journalJournal of Neurosurgeryen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US


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