The LMNA gene is involved in other monogenic diseases, especially Emery-Dreifuss muscular dystrophy, certain dilated cardiomyopathies, type-2B1 Charcot-Marie-Tooth neuropathy, type-A mandibuloacral dysplasia, restrictive dermopathy, Hutchison-Gilford progeria, as well as in numerous overlapping phenotypes between these different entities [20–22]. The gene discussed is LMNA; the disease is Charcot-Marie-Tooth disease, axonal, type 2FF.