Muscular dystrophy (MD) is an inherited (genetic) disorder of the muscles. It is called a neuromuscular disease. There are several types. Becker muscular dystrophy (BMD) is a rare type.
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Duchenne muscular dystrophy is a rare genetic condition that weakens your child's muscles. It appears in young boys, usually between ages 2 and 5.
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EDMD is a rare inherited muscle disease. It causes weakness in your child’s shoulders, upper arms, and calves. The disease also causes stiff joints that can’t move well.
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FSHD is a rare genetic muscle disease that affects the muscles of your child’s face, shoulders, upper arms, and lower legs.
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Spinal muscular atrophy (SMA) is a disease of the nerves and muscles caused by certain genes. It causes muscle wasting and weakness.
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