For example, mutations in LMNA (Patient ID 30 and 33) have been associated with many different phenotypes, including Emery–Dreifuss muscular dystrophy, Dunnigan‐type familial partial lipodystrophy, a form of dilated cardiomyopathy with conduction system disease, a form of familial partial lipodystrophy, limb‐girdle muscular dystrophy type 1B, a form of autosomal recessive axonal neuropathy (CMT), Hutchinson‐Gilford progeria syndrome, and mandibuloacral dysplasia (Mercuri et al., 2004). This evidence concerns the gene LMNA and familial partial lipodystrophy.