НЕСОВЕРШЕННЫЙ ОСТЕОГЕНЕЗ: ПОЛИМОРФИЗМ КЛИНИЧЕСКИХ ПРОЯВЛЕНИЙ И ТАКТИКА ЛЕЧЕНИЯ

Abstract

Osteogenesis imperfecta syndrome characterized by clinical manifestations of polymorphism under light for a long time can not be diagnosed, and it becomes apparent only after the symptoms found in children and grandchildren these patients. Management of patients with this nosology requires a multi-component approach in the context of the family with questions of prevention of recurrent fractures, treatment, rehabilitation and disability.

Keywords

• osteogenesis imperfecta
• connective tissue
• joint hypermobility