Autosomal recessive mutations in the DYSF gene cause muscular dystrophies (MD): a limb girdle MD, the so-called LGMD 2B, with onset in the proximal lower limbs [1], and two distal MD, one initially affecting the gastrocnemius muscle during early adulthood, Miyoshi myopathy (MM) [2], and the other involving muscles of the anterior compartment (DMAT) [3]. Here, DYSF is linked to Menkes disease.