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Muscular dystrophies are part of a group of degenerative diseases of the muscular system, which are characterized by muscle degeneration and structural changes at the neuromuscular junction. The most common form is Duchenne Muscular Dystrophy (DMD) (Whitehead et al., 2006), which affects approximately 1 in every 3500 live births (Balaban et al., 2005; Judge et al., 2005; Withehead et al., 2006; Radley et al., 2007). It is a severe X-linked recessive disorder, where the X chromosome is mutated in the region of the gene Xp21, which encodes for the production of dystrophin (Pearce, 2005).

Synaptic Changes at the Spinal Cord Level and Peripheral Nerve Regeneration During the Course of Muscular Dystrophy in MDX Mice