Status: Recruiting
Fibrous Dysplasia, McCune-Albright Syndrome Patient Registry
The FD/MAS Patient Registry is an IRB-approved research study that that invites the patients and families to help answer some of the biggest questions about FD/MAS by completing questionnaires about their lives with FD or MAS. Have you enrolled in the FD/MAS Patient Registry yet? Are you up-to-date on your surveys? Take a trip to www.fdmasregistry.org today to learn more about the project, enroll, complete your surveys, or make sure you aren't due to provide more info! The FD/MAS Patient Registry: Your story powers research.
Participants needed: 600
Trial details
Biological sex: AllType: ObservationalSponsor: Tovah BursteinUpdated: Aug 12, 2025Locations: 1Duration: 2 Years
Eligibility criteria
clinical diagnosis of fibrous dysplasia [+2]