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dc.contributor.authorYavuzer S.
dc.contributor.authorKara M.
dc.date.accessioned2020-06-25T15:13:18Z
dc.date.available2020-06-25T15:13:18Z
dc.date.issued2003
dc.identifier.issn15699293
dc.identifier.urihttps://doi.org/10.1016/S1569-9293(03)00127-0
dc.identifier.urihttps://hdl.handle.net/20.500.12587/1721
dc.description.abstractA cleft sternum is a rare congenital anomaly often diagnosed as asymptomatic at birth. Clinical outcome may be unfavorable when an associated anomaly, particularly an intracardiac anomaly coexists with the defect. Primary repair should be employed in the neonatal period because the flexibility of the chest wall is maximal and compression of underlying structures is minimal. However, patients with sternal cleft may even present late in the childhood or adolescence period. We herein report a case of a 4-year-old girl with sternal cleft who showed a favorable clinical outcome following successful primary surgical repair with the use of autogenous tissues. © 2003 Elsevier B.V. All rights reserved.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1016/S1569-9293(03)00127-0en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCongenital anomalyen_US
dc.subjectSternal cleften_US
dc.subjectSurgeryen_US
dc.titlePrimary repair of a sternal cleft in an infant with autogenous tissuesen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume2en_US
dc.identifier.issue4en_US
dc.identifier.startpage541en_US
dc.identifier.endpage543en_US
dc.relation.journalInteractive Cardiovascular and Thoracic Surgeryen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US


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