Scientists hunt for genetic fingerprint of rare bone disease
NCT ID NCT03838991
Summary
This study aimed to understand why fibrous dysplasia, a rare bone condition, varies so much in severity between patients. Researchers looked for tiny genetic markers in the blood and bone tissue of 24 adults with the disease. The goal was to identify markers linked to more severe disease, which could help future research but did not test a treatment.
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Contacts and locations
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Locations
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Service de Rhumatologie & INSERM U1033, Pavillon F, Hopital Edouard Herriot
Lyon, 69437, France
Conditions
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