The Dunnigan lipodystrophy variety, also known as familial partial lipodystrophy type 2 (FPLD2; OMIM151660), is a rare autosomal dominant disease, with an estimated prevalence of less than 1 in 10 million [3], which is caused by mutations in the LMNA gene, which is located in chromosome 1q21-22, encoding the nuclear proteins lamin A and C [12-14]. This evidence concerns the gene LMNA and familial partial lipodystrophy, Dunnigan type.