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Please contact:
Audrey Gordon
978-535-2594
info@progeriaresearch.org

Who Are We?
Hutchinson-Gilford Progeria Syndrome ("Progeria", or "HGPS") is a rare, fatal genetic condition characterized by an appearance of accelerated aging in children. Its name is derived from the Greek and means "prematurely old." Although they are born looking healthy, children with Progeria begin to display many characteristics of accelerated aging within the first two years of life.


Our Mission
To discover treatments and the cure for Hutchinson-Gilford Progeria Syndrome and its aging-related disorders, including heart disease.

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Progeria Research Foundation

P.O. Box 3453
Peabody, MA 01960
978-535-2594
www.progeriaresearch.org

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