hrp0084p3-664 | Bone | ESPE2015
, Hoyer-Kuhn Heike
, Allo Gabriel
, Schoenau Eckhard
Background: Osteogenesis imperfecta is a rare collagen related hereditary disease leading to recurrent fractures, reduced mobility, muscular weakness and short stature.Objective and hypotheses: It was always discussed if the reduced height is a consequence of the impaired collagen production, a reaction of the body to the brittleness of bones or if the patient might suffer from an additional deficiency of growth hormone (GH).Method...