Duchenne muscular dystrophy is a progressive muscle disorder for which pres
ently no specific drug therapy is available. Although many substances have
been tested only steroids demonstrated an increase of muscle mass and muscl
e force. The most frequently observed side effects include increase of weig
ht, hirsutism, and cushingoid appearance. Patients who may be considered fo
r steroids are patients older than five years who are still able to walk. A
new concept in managing muscular dystrophy is myoblast transfer therapy. A
lthough an increase of donor-derived dystrophin-positive fibers has been sh
own in the animal modell, placebo-controlled double-blind studies failed to
demonstrate any clinical improvement in Duchenne muscular dystrophy patien
ts.