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
Related Conference of Osteogenesis imperfecta
May 23-24, 2024
35th International Congress on Prevention of Diabetes and Complications
Zurich, Switzerland
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28th International Conference on Diabetes, Endocrinology and Healthcare
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Osteogenesis imperfecta Conference Speakers
Recommended Sessions
- Arthritis
- Bone Health
- Bone Tumours
- COVID-19 and arthritis
- Diagnosis of Osteoporosis
- Effect of COVID-19 on the Management of Osteoporosis
- Management of Osteoporosis in the Era of COVID-19
- Musculoskeletal Disorders
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- Osteonecrosis
- Osteopenia
- Osteoporosis
- Osteoporosis and Nutrition
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