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Up to: Osteogenesis imperfecta and a reduction of bone mineral density.
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type III is a severe type of osteogenesis imperfecta (OI), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures. The main signs of type III include very short stature, a triangular face, severe scoliosis, grayish sclera, and dentinogenesis imperfecta (DI).
This condition has no sub-types.