progeria

(redirected from Hutchinson Gilford Progeria Syndrome)
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progeria

[prō′jir·ē·ə]
(medicine)
An abnormal childhood state of premature senescence, characterized by wrinkled skin, gray hair, lack of pubic or facial hair, development of atherosclerosis, and a short life span. Also known as Hutchinson-Gilford syndrome.
References in periodicals archive ?
6] Nonstandard abbreviafions: CDG, congenital disorders of glycosylation; TIEF, transferrin isoelectric focusing; ApoC-III, apolipoprotein C-III; IEF, isoelectric focusing; Ga1NAc, N-acetylgalactosamine; NeuAc, sialic acid; FTC, familial tumoral calcinosis (MIM 211900); HIBM, hereditary inclusion body myopathy (MIM 600737); MEB, muscle-eye-brain disease (MIM 253280); HUS, hemolyfic uremic syndrome; HGPS, Hutchinson Gilford progeria syndrome (MIM 176670), F5FSD, a combined deficiency of factor V and factor VIII (MIM 227300); ER, endoplasmic reficulum; COG7, conserved oligomeric Golgi complex; CMP-NeuAc: cytidine 5'monophospho-N-acetylneuraminic acid; GNE/MNK, uridine-5'-diphosphate-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase; GALNT3, UDP-Ga1NAc transferase 3.
00pm THE four-year-old subject of this harrowing documentary is Hayley Okines, who suffers from an extremely rare genetic condition called Hutchinson Gilford Progeria syndrome.
London, June 6 (ANI): A seven-year old Brit girl has the face and body of an old woman as she suffers from a rare genetic disorder called Hutchinson Gilford Progeria Syndrome.