Welcome
Why Choose Us
We understand that finding out that you or a loved one has a rare bone disorder can be overwhelming. These rare bone disorders, such as Osteogenesis Imperfecta (OI), Hypophosphatasia (HPP), X-linked hypophosphatemic rickets (XLH), Fibrodysplasia Ossificans Progressiva (FOP), or Tumor-Induced Osteomalacia (TIO) and others, are the focus of our program, which provides care across the lifespan from infants to adults. This clinic is unique in that it treats entire families with these lifelong conditions.
Our team is led by knowledgeable physicians and staff who are developing innovative research in order to develop guidelines to treat these ultra-rare and chronic diseases.
Get a pulse
Regular visits and taking care of your health are of the utmost importance. Schedule a visit or contact us today!
Medical Counseling
Reach out to us to discuss your concerns and we will work together to get you the best health care possible.
Our Team
We leverage our resourceful and collaborative medical team to ensure effective and friendly health care.
Heredity & Families
Our medical team works with individuals or whole families, or we start with one and bring others on later.
Our
Founders
Our vision is to provide exceptional medical care and world-class discovery opportunities for individuals and families with hereditary bone disorders across the lifespan by bridging resources across the Vanderbilt Medical Center.
Kathryn McCrystal Dahir, MD
Physician, Professor of Medicine
Department of Endocrinology
Vanderbilt University Medical Center
Jill Simmons, MD
Physician, Professor of Pediatrics
Division of Pediatric Endocrinology and Diabetes
Vanderbilt University Medical Center
A cohesive and dedicated team is here to help you and your family manage chronic bone diseases.
We understand that finding out that you or a loved one has a rare bone disease can be overwhelming. |
This clinic is unique in that it treats entire families with lifelong conditions. |