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- W2034176749 abstract "Hutchinson-Gilford progeria syndrome (HGPS) is a rare and fatal genetic disorder that results in accelerated atherosclerosis and signs and symptoms of rapid aging. The incidence has been estimated at approximately 1 in 4 million births.1 Children with HGPS have failure to thrive, alopecia, thinning of skin, loss of body fat, headaches, atherosclerosis, cardiovascular disease, and stroke. Death occurs at an average age of 13 years and most commonly results from myocardial infarction or stroke." @default.
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- W2034176749 date "2013-06-28" @default.
- W2034176749 modified "2023-09-23" @default.
- W2034176749 title "Moving from gene discovery to clinical trials in Hutchinson-Gilford progeria syndrome" @default.
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- W2034176749 doi "https://doi.org/10.1212/wnl.0b013e31829d87cd" @default.
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