Tag: Hutchinson-Gilford Progeria Syndrome

Hutchinson-Gilford Progeria Syndrome (HGPS) Definition and Description of Hutchinson-Gilford Progeria Syndrome (HGPS) Hutchinson-Gilford Progeria Syndrome (HGPS) is an extremely rare genetic disorder characterized by accelerated aging in children. The term “progeria” comes from Greek, meaning “prematurely old.” HGPS is caused by a mutation in the LMNA gene, which produces the Lamin A protein essential for…