17/08/2026
Osteogenesis Imperfecta: Types, Symptoms, Tests & Treatment - Pediatric
Osteogenesis Imperfecta, commonly called brittle bone disease, is a rare inherited connective tissue disorder characterized by fragile bones that fracture easily. The condition primarily results from abnormalities in type I collagen production or structure, leading to weakened bones and connective tissues.
The severity of osteogenesis imperfecta (OI) varies widely. Some individuals experience only a few fractures during their lifetime, while others may suffer hundreds of fractures, skeletal deformities, respiratory complications, hearing loss, and mobility impairment.
Read More: https://orthofixar.com/pediatric/osteogenesis-imperfecta-oi-types-treatments/