Osteogenesis imperfecta

Osteogenesis imperfecta (OI) is a category of bone-related hereditary diseases. The word "osteogenesis imperfecta" refers to a defect in the creation of bones. Bones in people with this condition are prone to breaking (fracture), often as a result of minor trauma or for no apparent reason. Multiple fractures are common and can occur even before birth in severe cases. Milder instances may only result in a few fractures throughout the course of a person's life.

  • Type I Osteogenesis imperfecta
  • Type II Osteogenesis imperfecta
  • Type III Osteogenesis imperfecta
  • Type IV Osteogenesis imperfecta
  • Type V Osteogenesis imperfecta
  • Type VI Osteogenesis imperfecta
  • Type VII Osteogenesis imperfecta
  • Type VIII Osteogenesis imperfecta

 

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