What Is Muscular Dystrophy?

Muscular dystrophies are genetic conditions. Patients with muscular dystrophy can inherit the condition from their parents, or be the first in their family to have symptoms. It is not a single disease but a group of over 30 conditions involving muscle function. All types of muscular dystrophy are considered neuromuscular diseases because they affect the way nerves and muscles work together to create body movements.

Muscular Dystrophy Care at Stanford

Stanford is a recognized leader in muscular dystrophy care and research. We hold an MDA Clinic designation from the Muscular Dystrophy Association.

At Stanford, our Neuromuscular Program doctors also work closely with colleagues in the Center for Inherited Cardiovascular Disease and other specialty clinics to optimize care for muscular dystrophy. For muscular dystrophies that occur in childhood, our pediatric and adult cardiologists work together to ensure that patients transition smoothly from pediatric to adult clinics.

Learn more about our Neuromuscular Program and Center for Inherited Cardiovascular Disease.

How is Muscular Dystrophy Treated?

At Stanford, we take a comprehensive approach to muscular dystrophy treatment. Your care team will include a team of experienced subspecialists, from physical therapists and respiratory therapists to genetic counselors. Read more about muscular dystrophy treatment at Stanford.