Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report

• Egile Nagusiak: Priyanka Kant (Egilea), Neelkamal Sharda (Egilea), Rahul R. Bhowate (Egilea)
• Formatua: Liburua
• Argitaratua: Hindawi Limited, 2013-01-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Osteopetrosis is a rare inherited genetic disease characterized by sclerosis of the skeleton caused by the absence or malfunction of osteoclasts. Three distinct forms of the disease have been recognized, autosomal dominant osteopetrosis being the most common. Autosomal dominant osteopetrosis exhibit...