Progeria is a rare genetic condition characterized by an appearance of accelerated aging in children. Its name is derived from the Greek and means "prematurely old." The classic type is the Hutchinson-Gilford Progeria Syndrome which was first described in England in 1886 by Dr. Jonathan Hutchinson and again in 1886 and 1904 by Dr. Hastings Gilford.- Category ID : 75944
Images of persons with this disease and diagnostic criteria for WRN and contact information for a central repository of WS data and research and materials.
Information and photos about a child with the rare genetic disorder Hutchinson Gilford Progeria Syndrome. Including photographs, media articles and links to related sites.