In 2006, Verstraeten et al. [2] reported a male affected by a progeroid syndrome with two LMNA missense variants: c.1619T>C, p.(Met540Thr) in exon 10, inherited from his mother, and c.1583C>T p.(Thr528Met) in exon 9, inherited from his father. The gene discussed is LMNA; the disease is progeroid syndrome.