LMNA and Hutchinson-Gilford progeria syndrome: Mutations in the LMNA gene have many implications leading to various manifestations of autosomal dominant and recessive conditions such as dilated cardiomyopathy, Emery-Dreifuss muscular dystrophy, congenital muscular dystrophy, Charcot Marie Tooth Disease, and Hutchinson-Gilford progeria syndrome (4).