"A genetic or heritable condition is osteogenesis imperfecta (OI), in which bones are soft and fracture (break) readily, with no apparent cause or slight injury. The disorder can be mild, with only a few fractures occurring in a lifetime. In more severe instances, it can also entail hundreds of fractures that happen for no apparent reason. The treatment of osteogenesis imperfecta is to strengthen the bones, physiotherapy to relieve pain, and orthopedic surgery. "
Radiographic Characteristics of Rare Pediatric Musculoskeletal Disorders
Radiological imaging helps in guiding healthcare professionals toward an accurate diagnosis of rare pediatric musculoskeletal disorders.
Osteogenesis Imperfecta - Types, Symptoms, Manifestations, Diagnosis and Treatment
Osteogenesis imperfecta (OI) is a heterogeneous group of genetic diseases with a predominantly autosomal dominant pattern of inheritance.
