Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic condition where children undergo premature aging. Characterized by the appearance of aging-related effects like hair loss, wrinkled skin, cardiovascular disease, and stiffness of joints, HGPS affects approximately one in eight million newborns worldwide. Children with HGPS generally live to an average age of 14.5... https://justpaste.me/pl5g