DMD and limb-girdle muscular dystrophy: After receiving negative results of MLPA aimed at the detection of <i>DMD</i> deletions and duplications, as well as the limb-girdle muscular dystrophy gene panel sequencing, the patients were referred to whole genome sequencing, which allowed to detect a translocation involving the short arm of the X chromosome and with breakpoints in the <i>DMD</i>.