Osteogenesis Imperfecta (OI) is a genetic disorder, also known as the “brittle bone disease”, associated with an increased bone fragility. Several phenotypes exist, reflecting different severities but some features are frequently observed like a reduced stature and long bone deformities. A few treatments are currently used but none of them is curative. To improve those treatments there is a need for a better understanding of the mechanisms involved. Therefore, the objective of this work is to investigate the effects of OI on the bone tissue at macroscopic and tissue scales. The main interest of this project is to perform a comparative study between a group of OI bones retrieved from children with OI and a group of control bones retrieved fr...