Skin signs as early manifestations of Hutchinson-Gilford progeria syndrome
Archives of Diseases in Childhood, 06/26/2012
D’Erme AM et al. – Hutchinson–Gilford progeria syndrome (HGPS) is a rare, sporadic, autosomal dominant genetic disorder with phenotypic features of accelerated ageing due to a mutation of the lamin A (LMNA) gene.



