Hutchinson–Gilford progeria syndrome (HGPS) is a lethal disease caused by the autosomal dominant de novo mutation (1824C > T, p.G608G) in exon 11 of the Lamin A (LMNA) gene that activates a splicing donor site resulting in the production of Progerin, a toxic LMNA variant [1, 2] that leads to premature aging features [3, 4]. Here, LMNA is linked to Hutchinson-Gilford progeria syndrome.