FD/MAS PATIENT REGISTRY

The FD/MAS Patient Registry is a research project that allows patients and families to share their experiences with fibrous dysplasia/McCune-Albright syndrome (FD/MAS) by completing a series of surveys... If you're located in the United Kingdom, please visit https://research.ndorms.ox.ac.uk/rudy/ to learn about the RUDY study, the FD/MAS registry based in the UK.

Also known as: FD/MAS