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dc.contributor.authorAnarat, Fikret Berkan
dc.contributor.authorBayram, Serkan
dc.contributor.authorErgin, Ömer Naci
dc.contributor.authorMert, Lezgin
dc.contributor.authorChodza, Mechmed
dc.date.accessioned2021-03-03T19:56:18Z
dc.date.available2021-03-03T19:56:18Z
dc.date.issued2018
dc.identifier.citationBayram S., Mert L., Anarat F. B. , Chodza M., Ergin Ö. N. , "A Newborn With Multiple Fractures in Osteogenesis Imperfecta: A Case Report", Journal of Orthopaedic Case Reports, cilt.8, sa.3, ss.71-73, 2018
dc.identifier.othervv_1032021
dc.identifier.otherav_5730ab2b-8102-4e8f-a001-e5f42741dfc5
dc.identifier.urihttp://hdl.handle.net/20.500.12627/61515
dc.identifier.urihttps://doi.org/10.13107/jocr.2250-0685.1116
dc.description.abstractIntroduction:Multiple bone fractures in a newborn can be associated with osteogenesis imperfect (OI). OI is a rare genetic disorder that causes Type I collagen synthesis disturbance results in bone fragility.Case report:We present a female newborn which had numerous fractures of the humerus, bilateral clavicle, and bilateral femur. Her delivery was at 36 weeks gestation by spontaneous vaginal delivery. She had has not any pathological symptom at 2 weeks after birth, the patient had a fracture of the humerus, bilateral clavicle, and femur without any trauma. Genetic analysis of the patient was reported and OI diagnosed. The patient was followed up for 8 months with regularly and without any complication.Conclusion:Multiple fractures with OI in an infant after birth may require an accurate orthopedic plan for diagnosing and treatment.
dc.language.isoeng
dc.subjectOrtopedi ve Travmatoloji
dc.subjectTıp
dc.subjectCerrahi Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectORTOPEDİ
dc.subjectCERRAHİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.titleA Newborn With Multiple Fractures in Osteogenesis Imperfecta: A Case Report
dc.typeMakale
dc.relation.journalJournal of Orthopaedic Case Reports
dc.contributor.department, ,
dc.identifier.volume8
dc.identifier.issue3
dc.identifier.startpage71
dc.identifier.endpage73
dc.contributor.firstauthorID1379024


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