New insight into 'accelerated aging' disease
Monday, September 13, 2010 - 13:15
in Health & Medicine
Hutchinson-Gilford Progeria Syndrome (HGPS or progeria) is a rare genetic disease that causes young children to develop symptoms associated with advanced age, such as baldness, wrinkles, osteoporosis and cardiovascular disease. Now, a study uses a mouse model to shed light on progeria, and perhaps also on the normal aging process.