Duchenne muscular dystrophy (DMD) is considered the most common serious form of muscular dystrophy; it is attributed to nonsense or frame-shift mutations in the X chromosome DMD gene encoding the dystrophin protein that leads to loss of expression and a lethal muscle-wasting disorder, which is estimated to impact approximately 1/3500–5000 male births worldwide [1,2]. This evidence concerns the gene DMD and Duchenne muscular dystrophy.