Background Osteogenesis imperfecta (OI) is a hereditary genetic disorder characterized by
bone fragility and extremity deformities. The surgical management for long-bone fractures …

Introduction The most commonly accepted method of long bone deformity correction in
children with osteogenesis imperfecta is surgical realignment with transphyseal telescopic …

Objective: Intramedullary rodding of lower extremity long bones in patients with
osteogenesis imperfecta (OI) is a widely accepted technique for fracture treatment and …

(1) Background: The Fassier–Duval (FD) nail was developed for the treatment of
osteogenesis imperfecta (OI). The aim of this study was to review the results of OI patients …

Background: Osteogenesis imperfecta (OI) is a genetic disorder characterized by brittle
bones and long bone deformity. Realignment and intramedullary rodding with telescopic …

Background: Osteogenesis imperfecta (OI) is a genetic defect in collagen type I,
phenotypically characterized by bony fragility and a propensity to high rates of childhood …

Methods Twenty-three patients who were operated on for the diagnosis of osteogenesis
imperfecta between 2005 and 2018 were retrospectively analyzed. Demographic data …

Methods: A retrospective chart review was performed on pediatric patients treated at a
tertiary care center across a 15-year period. Inclusion criteria to select patients was:(1) …

Osteogenesis Imperfecta (OI) is a rare genetic disorder in Type I collagen characterized by
bone fractures, fragility, and deformity. Current treatments are focused on decreasing …

Обоснование. Основным ортопедическим проявлением несовершенного остеогенеза
(НО) являются множественные переломы, которые приводят к неправильному …