The purpose of the Fragile Bone Registry is to gather as much information as we can about patients as possible who have osteopenia, osteoporosis, or a history of a low energy fracture. This will facilitate investigators in developing a better understanding of the clinical features, pathobiology, and genetic links associated with fragile bones. With this increased knowledge, investigators hope to identify the unmet needs of patients with fragile bones and develop new and better treatments to improve disease outcomes and quality of life. Patients will be asked to allow researchers to gather information about their background and medical history, and gather clinical information on them. Approximately 600 patients will be enrolled during the course of this registry. Patients will be followed-up on a yearly basis
Inclusion criteria:
Exclusion criteria:
Joseph M.Lane, MD
212.606.1172
lanej@hss.edu
Ania Rodney (Research Coordinator)
212.606.1604
rodneya@hss.edu
©2008 Hospital for Special Surgery. 535 East 70th Street, New York, NY 10021