Explore: Osteogenesis Imperfecta, Congenital Anomalies
Osteogenesis Imperfecta is disease in which the bones are not properly formed and break easily. It also know as Brittle Bone disease or OI. People with this disease are generally short, and may be dwarfs....
This page was last updated on October 11th, 2008
This page was last updated on October 11th, 2008
Osteogenesis Imperfecta (from Congenital Anomalies)
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Osteogenesis Imperfecta: The Links to Nutrition
Reviews the possible role of nutrition in this disorder. Questions whether it is solely a genetic condition.
Osteogenesis imperfecta hub
Links to overviews, clinical trials, images, research articles and abstracts for osteogenesis imperfecta.
The Bone Page
Bisphosphonate FAQ, bone density, and other information for families dealing with OI.
Osteogenesis Imperfecta Federation Europe
Information on Osteogenesis Imperfecta around Europe
Brittle Bone Society
The UK charity providing support for people with osteogenesis imperfecta.
The Osteogenesis Imperfecta Mailing List
For the discussion of any issues relating to OI. Open to both professionals and families.
Children's Brittle Bone Foundation Website
US organization. Online grant and fellowship applications with news about recent and upcoming events.
Osteogenesis Imperfecta
Article from eMedicine.
Osteogenesis Imperfecta Foundation
Supports and encourages medical research and disseminates information to patients, their families, and medical professionals
Osteogenesis Imperfecta Information
Resources gathered by the mother of a child with the disease. Includes a personal page about her son Jojo, his disease, treatment, and progress.
Reviews the possible role of nutrition in this disorder. Questions whether it is solely a genetic condition.
Links to overviews, clinical trials, images, research articles and abstracts for osteogenesis imperfecta.
Bisphosphonate FAQ, bone density, and other information for families dealing with OI.
Information on Osteogenesis Imperfecta around Europe
The UK charity providing support for people with osteogenesis imperfecta.
For the discussion of any issues relating to OI. Open to both professionals and families.
US organization. Online grant and fellowship applications with news about recent and upcoming events.
Article from eMedicine.
Supports and encourages medical research and disseminates information to patients, their families, and medical professionals
Resources gathered by the mother of a child with the disease. Includes a personal page about her son Jojo, his disease, treatment, and progress.
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