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Osteogenesis imperfecta (OI) is probably the most common genetic form of fracture predisposition. The term OI encompasses a broad range of clinical presentations that may be first apparent from early ...
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Background Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in the genes involved in the production of type 1 collagen. OI is also known as brittle bone disease.
Bjørn Magne Jåtun, specialist in paediatrics and senior consultant in charge of endocrinology and local follow-up of children with osteogenesis imperfecta. The author has completed the ICMJE form and ...
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