National Registry of Myotonic Dystrophy and Facioscapulohumeral Muscular
Dystrophy Patients and Family Members
The National Registry was developed to:
- Help people with Myotonic Dystrophy (DM) or Facioscapulohumeral Muscular
Dystrophy (FSHD) participate in research on their disease.
- Help investigators accomplish their research by connecting them with
people who have DM or FSHD.
- Encourage more research on these rare diseases.

This project has been funded in whole or part by Contract #N01-AR-50-227450
from the National Institute of Arthritis and Musculoskeletal and
Skin Diseases (NIAMS) and the National Institute of Neurologic Disorders
and Stroke (NINDS).

dystrophy_registry@urmc.rochester.edu
Updated 9/12/2006