Long-term study of bone fragility in osteogenesis imperfecta
Part of Bones, joints & muscles, Genetic & congenital, Skin clinical trials.
This study follows people with osteogenesis imperfecta (OI) to better understand how it affects bones and related issues over time. It may help doctors learn which features and genetic changes predict problems, and guide future care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have a confirmed OI diagnosis by DNA testing, or your X-rays and history strongly suggest OI
- You can return for scheduled follow-up visits
- You do not have another genetic condition or syndrome that also explains your bone findings
- You have no other bone-related disorder besides OI (unless the study specifically allows it)
- If you join the spine/scoliosis part, you’re ages 3–17, or 18+ with scoliosis
- If you join the dental/craniofacial part, you’re age 3+ and agree to a dental exam
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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