Pediatric Neuromuscular Disease Program
Expert Care for Neuromuscular Disease
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Meet the Care Team
Patient Stories
Harrison's story: How gene therapy could help against Duchenne muscular dystrophy
When Pam first heard about gene therapy, she thought it sounded like science fiction. She never would have guessed her son would be among the first patients to receive an innovative new gene therapy that's giving new hope against Duchenne Muscular Dystrophy (DMD).

Conditions We Treat
Pediatric Charcot-Marie-Tooth disease (CMT)
Pediatric chronic inflammatory demyelinating polyneuropathy (CIDP)
Congenital myopathy
Pediatric Guillain-Barré syndrome (GBS)
Muscular dystrophy (MD) in children
Myasthenia gravis (MG) in children
Pediatric myotonic dystrophy
Spinal muscular atrophy (SMA) in children
Pediatric hypotonia (floppy muscle syndrome)
Pediatric neuromuscular disorders
Pediatric polyneuropathy cognitive disorders
Muscle weakness in children
More Details
At Children's Health℠, we work with babies and children who have a wide range of conditions that affect their nerves and muscles. Some neuromuscular diseases are genetic, and others may be caused by injuries, autoimmune diseases or infections. These diseases can affect different groups of muscles and different kinds of nerves.
Children’s Health has one of the nation’s largest programs for pediatric neuromuscular medicine. We offer the latest diagnostic tools and treatments for these rare and complex conditions. Our affiliation with UT Southwestern means your child may also be able to join research studies that give them access to new treatments.