We are pleased to announce the launch of FD/MAS Patient Registry! The FD/MAS Patient Registry creates a platform for patients around the world to strengthen their voices and share information about Disease, a disease that causes . fibrous dysplasia, McCune-Albright syndrome (FD/MAS) currently has no cure. Designed with the input of scientists and patients, this global resource will provide data for researchers to use to advance drug development and treatment options to help improve fibrous dysplasia, McCune-Albright syndrome (FD/MAS) patient care. Join now and let your data tell your story!