Clinic Case of Rare Type VI Osteogenesis Imperfecta

• Egile Nagusiak: Olga N. Ignatovich (Egilea), Leyla S. Namazova-Baranova (Egilea), Tea V. Margieva (Egilea), Natalia V. Zhurkova (Egilea), Kirill V. Savostyanov (Egilea), Alexander V. Pushkov (Egilea)
• Formatua: Liburua
• Argitaratua: Union of pediatricians of Russia, 2019-04-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Osteogenesis imperfect is genetically heterogeneous group of diseases which are characterized by bone brittleness and fractures. It was thought for a long time that this is happening due to mutations in collagen genes. However, within past decade the understanding of osteogenesis imperfecta etiology...