ba0005p472 | Paediatric bone disease | ECTS2016
Nassar Kawtar
, Janani Saadia
, Rachidi Wafae
, Mkinsi Ouafa
, Cherqaoui Abdelmounim
, Aboumaarouf M
Introduction: Osteogenesis imperfecta is a rare constitutional bone disease. The bone matrix is poor because of the often mutation on the gene coding for collagen I, leading to many fractures. Classification Sillence completed by Glorieux, describes the clinical variability. The management should be done case by case.Study objective: Evaluate the clinical profile, biological and radiological of 5 newly diagnosed cases.Material and ...