Mutations in the Lamin A/C gene have been shown to cause several inherited diseases known as laminopathies [15], ranging from more tissue-specific, such as Emery-Dreifuss muscular dystrophy or cardiomyopathy, to more generalized pathologies, such as atypical Werner Syndrome(WS) and Hutchinson-Gilford Progeria Syndrome (HGPS) [16–21]. This evidence concerns the gene LMNA and Hutchinson-Gilford progeria syndrome.