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dc.contributor.authorGöçer H.
dc.contributor.authorUlusoy S.
dc.contributor.authorÇirakli A.
dc.contributor.authorKaya I.
dc.contributor.authorDabak N.
dc.date.accessioned2020-06-21T09:37:55Z
dc.date.available2020-06-21T09:37:55Z
dc.date.issued2014
dc.identifier.issn1302-0072
dc.identifier.urihttps://doi.org/10.4274/Haseki.1422
dc.identifier.urihttps://hdl.handle.net/20.500.12712/4839
dc.description.abstractOsteogenesis imperfecta is a hereditary disorder characterized by increased bone fragility. The production of type I collagen and endochondral bone development are disturbed. The disease is also considered a systemic syndrome affecting several organs besides skeletal system. Here, we present a case of osteogenesis imperfecta in a 13-year-old child with femoral fracture after a minor trauma on his left femur and ipsilateral deformity that were treated simultaneously by locked intramedullary nailing. Furthermore, the deformity on the right femur was treated using the same technique three months later. In this paper, the treatment of fractures and deformity correction in patients with osteogenesis imperfecta using locked intramedullary nailing technique is discussed in the light of the literature.en_US
dc.language.isoengen_US
dc.publisherGalenos Yayinevi Tic. Ltd. Sti.en_US
dc.relation.isversionof10.4274/Haseki.1422en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectDeformityen_US
dc.subjectFractureen_US
dc.subjectIntramedullary nailen_US
dc.subjectOsteogenesis imperfectaen_US
dc.titleIntramedullary nailing of deformity and fracture in a patient with osteogenesis imperfectaen_US
dc.title.alternativeOsteogenezis İmperfektalı hastada İntramedüller çivi ile kırık ve deformite tedavisien_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume52en_US
dc.identifier.issue2en_US
dc.identifier.startpage126en_US
dc.identifier.endpage129en_US
dc.relation.journalHaseki Tip Bultenien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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