There is no cure for any form of muscular dystrophy, but medications and therapy can slow the course of the disease. Human trials of gene therapy with the dystrophin gene are on the near horizon. For instance, scientists are researching ways to insert a working dystrophin gene into the muscles of boys with Duchenne and Becker muscular dystrophies. read more
Duchenne muscular dystrophy (DMD) is associated with the most severe clinical symptoms as compared to Becker muscular dystrophy (BMD) which has milder symptoms. Calling it DMD the therapy is aimed at initial treatment with Glucocorticoids as the mainstay, and are offered for patients four years of age and older whose motor skills have plateaued or are declining. read more