hrp0086p1-p142 | Bone & Mineral Metabolism P1 | ESPE2016
Rehberg Mirko
, Semler Oliver
, Hoyer-Kuhn Heike
, Schonau Eckhard
, Winzenrieth Renaud
Background: Osteogenesis imperfecta (OI) is a hereditary connective tissue disorder due to mutations related to collagen type 1. OI presents itself with low bone mass, resulting in high bone fragility. Bone mass is relevant for determination of the severity of OI. Although bisphosphonate treatment is able to increase areal bone mineral density (aBMD) measured by DXA, there is no correlation to fracture rates.Objective and hypotheses: The aim of this stud...