Home > Health > Conditions and Diseases > Genetic Disorders > Progeria
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.
http://www.hayleyspage.com/
Information and photos about a child with the rare genetic disorder Hutchinson Gilford Progeria Syndrome. Including photographs, media articles and links to related sites.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Progeria,+Hutchinson+Gilford
Outlines the symptoms and lists related organizations.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Werner+Syndrome
Offers alternative names, a general discussion and further resources.
http://courses.cit.cornell.edu/psych527_nbb420-720/student2005/ljh34/hg.htm
Provides information on this rare disorder, its symptoms, genetics and treatments.
http://courses.cit.cornell.edu/psych527_nbb420-720/student2005/ljh34/werner.htm
Provides information on this rare disorder, its symptoms, genetics and treatments.
http://www.progeriaresearch.org/
Medical research, education, support, and fundraising for this "pre-mature aging" disease.
http://www.pathology.washington.edu/werner/
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.
http://en.wikipedia.org/wiki/Hutchinson-Gilford
Encyclopedia article on this rare genetic disorder, its causes, diagnosis, treatment, prognosis and research.
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