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Hutchinson-gilford progeria syndrome otherwise known as progeria (meaning prematurely old)(case study) or hgps, is a severe genetic disorder hgps was initially reported in 1886 by hutchinson and gilford in england(case) hgps is extremely rare. View essay - biology progeria essay from biology biology at bowie high school progeria progeria, or hutchinson-gilford syndrome, is an extremely rare autosomal dominant genetic disorder. Hutchinson-gilford progeria syndrome (hgps) is an extremely rare hereditary disease that affects the skin, musculoskeletal system, and vasculature hgps is characterized by signs of premature aging. This essay summarizes advances made in the study of lamin biology because despite cells in hutchinson- gilford progeria syndrome is due to the.
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