Osteogenesis Imperfecta

By | May 20, 2012

Osteogenesis Imperfecta (OI) or brittle bone disease is a group of autosomal dominant inherited disorders with abnormality in Type 1 collagen.[1], which usually result in bone fragility[2].


Frequency of OI in USA and worldwide, clinical features, laboratory diagnosis, classification and differential diagnosis.

The Cleveland Clinic

Explains the types and management of the Osteogenesis Imperfecta (OI) .


Explained in detail about clinical classification and phenotype, – Pediatric Imaging Teaching Files

Clinical trials for OI

Bisphosphonate Treatment of Osteogenesis Imperfecta