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].
Emedicine
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) .
Endtext
Explained in detail about clinical classification and phenotype, – Pediatric Imaging Teaching Files
Bisphosphonate Treatment of Osteogenesis Imperfecta