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Autor:
Ayşe Pınar Öztürk, Aslı Dudaklı, Esin Karakılıç Özturan, Şükran Poyrazoğlu, Firdevs Baş, Feyza Darendeliler
Publikováno v:
Klinische Pädiatrie. 234:199-205
Osteogenesis imperfecta (OI) is a genetic disease characterized by fragile bones and variable short stature.We performed a retrospective cohort study to evaluate demographic data, clinical findings, growth and pubertal characteristics, and medical tr