Scientists track Children's brittle bone disease to unlock genetic secrets
NCT ID NCT03575221
Summary
This study aimed to understand how osteogenesis imperfecta (brittle bone disease) develops over time in children and how different genes affect the symptoms. Researchers followed 46 children under age 12 with certain types of the condition, conducting regular check-ups and tests over several years. The goal was to gather detailed information about the disease's natural course to help improve future care, not to test a treatment.
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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Conditions
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