Osteogenesis Imperfecta (OI), often called "brittle bone disease, " is a rare genetic condition that makes bones very fragile. It's caused by a problem with a type of collagen, which affects different tissues in the body. Because OI impacts many body systems, people with it need care from many doctors.

Kids with OI get a lot of attention and treatments, like medicines and surgeries. But as they grow up, the focus often shifts. There aren't as many clear guidelines for adults with OI, especially when it comes to moving from children's care to adult care. Doctors from different fields need to work together to help OI patients manage their health during this big change.

A recent review looked at how OI patients, and those with other long-term diseases, experience switching from pediatric to adult care. The study followed strict rules called PRISMA to find the best and most relevant information.

Making this transition smooth requires planning and teamwork. Doctors from many specialties, like orthopedics, heart health, and mental health, must collaborate. Patients need to be educated and have personalized plans tailored to their needs. More research is needed to see how well these step-by-step transition plans work for OI patients.

Growing Up with Brittle Bones: How Osteogenesis Imperfecta Patients Transition to Adult Care

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