Osteogenesis Imperfecta Symptoms, Cause, Genetics, Radiology & Treatment | Brittle Bone Disease
In this video I will tell you about Osteogenesis Imperfecta. Osteogenesis imperfecta is a rare genetic connective tissue disease characterized by multiple and recurrent fractures. The severe fetal type (osteogenesis imperfecta
congenita) is characterized by multiple intrauterine or perinatal fractures. Moderately affected children have numerous fractures and are dwarfed as a result of bony deformities and growth retardation. Intelligence is not affected. The shafts of the long bones are reduced in cortical thickness, and wormian bones are present in the skull. Other features include blue scleras, thin skin, hyperextensibility of ligaments, otosclerosis with significant hearing loss, and hypoplastic and deformed teeth.
Disclaimer: This video is only for education. Please consult your healthcare provider for diagnosis and management of medical conditions.
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