Osteogenesis Imperfecta (Type IV) with Dental Findings in Siblings

• Egile Nagusiak: Shishir Ram Shetty (Egilea), Deepa Dsouza (Egilea), Subhas Babu (Egilea), Preethi Balan (Egilea)
• Formatua: Liburua
• Argitaratua: Hindawi Limited, 2011-01-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Osteogenesis imperfecta (OI) is a hereditary disorder characterized by increased tendency for bone fractures due to high fragility. The clinical and radiological features of OI manifest in different age groups, although the disease is congenital in nature. Besides bone fragility, features like laxit...