GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS, cilt.15, ss.1-5, 2017 (Hakemli Dergi)
Introduction: Osteogenesis imperfecta (OI) is a hereditary disease that impairs the quality of life by frequent bone fractures. The objective of our study is to retrospectively evaluate patients diagnosed with OI and to come up with helpful data that will assist developing new diagnosis and treatment protocols.