ASSOCIATION OF BILATERAL RADIOULNAR SYNOSTOSIS WITH OSTEOGENESIS IMPERFECTA TYPE 1 - CASE PRESENTATION

• Main Authors: Valeriu V. Lupu (Author), Mirabela Subotnicu (Author), Ancuța Ignat (Author), Gabriela Păduraru (Author), Irina Naumcieff (Author), Bogdan Ciubară (Author), Marin Burlea (Author)
• Format: Book
• Published: Romanian Society of Oral Rehabilitation, 2016-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Osteogenesis imperfecta (OI) is a group of rare congenital conditions characterized mainly by bone brittleness secondary to mutations in the genes encoding collagen. The medical history together with a clinical examination in detail of the fractures is highly important in directing the diagnosis tow...