Progeria Research Foundation conducts the support of Medical Research, Promotion of Education and Awarness, and Fundraising ...

Welcome... Hutchinson-Gilford Progeria Syndrome is an extremely rare genetic disease that accelerates the aging process to about seven times the normal rate. Because of this accelerated aging, a child of ten years will have similar respiratory, cardiovascular, and arthritic conditions that a 70-year-old would have. Currently, there is no cure for this disease, and because of its rare nature, no ...

Genes and disease provides short descriptions of inherited disorders. It is hosted by the National Center for Biotechnology Information (NCBI), a division of the National Library of Medicine (NLM) at the National Institutes of Health (NIH).

Small collection of progeria cell line graphics