Tag: Hutchinson-Gilford

Read more Hutchinson-Gilford Progeria Syndrome, often simply called Progeria, is a rare genetic disorder affecting approximately 1 in every 4 to 8 million newborns. This condition is characterized by symptoms of rapid aging in children. The most recognized variant is Hutchinson-Gilford Progeria Syndrome. Symptoms of Progeria Children diagnosed with Progeria typically appear healthy at birth,…