Osteogenesis imperfecta pathophysiology
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Overview
Pathophysiology
Pathophysiology
As a genetic disorder, OI is an autosomal dominant defect. Most people with OI receive it from a parent but it can also be an individual (de novo or “sporadic”) mutation.
Looking for the patient version?
© 2026 MyEClinic – IFTM Institut für Telematik in der Medizin GmbH