Many genetic mutations in the lamin A/C gene result in human diseases, such as Emery Dreifuss muscular dystrophy (EDMD), cardiomyopathy dilated (CDM1A), Dunnigan-type familial partial lipodystrophy (FPLD), and Hutchinson-Gilford progeria syndrome (HPGS) [28,29,30,31,32]. This evidence concerns the gene LMNA and Emery-Dreifuss muscular dystrophy.