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The following 4 types of Osteogenesis Imperfecta have been reported ...
Type I is the most common and mildest form of Osteogenesis Imperfecta. While the structure of the collagen is normal, there is less collagen than there should be. There is little or no bone deformity, although the bones are fragile and easily broken. People with Type I Osteogenesis Imperfecta average nearly 40 fractures before puberty; however, they experience only a few fractures after puberty.
The effects of Osteogenesis Imperfecta may extend to the teeth, making them prone to cavities and cracking. The whites of the eyes may have a blue, purple, or gray tint.
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