LMNA and laminopathy: Today, over 450 variants have been identified in the LMNA gene that result in a wide range of inherited human “laminopathies”, including familial partial lipodystrophy of the Dunnigan variety, puberty-onset generalised lipodystrophy, limb-girdle muscular dystrophy, restrictive dermopathy, Emery–Dreifuss muscular dystrophy, Hutchison–Gilford progeria syndrome, and dilated cardiomyopathy [4].