Understanding Hutchinson-Gilford Progeria Syndrome
Hutchinson-Gilford Progeria Syndrome, also known as Progeria, is a rare genetic disease that causes premature aging in children. Progeria affects about one in four million newborns worldwide and has no cure. Children with Progeria usually live until their early teens, but some may survive into their twenties. What are the symptoms of Progeria? Progeria is … Read more