早年衰老症候群 - 维基百科，自由的百科全书
早年衰老症候群（Hutchinson-Gilford Progeria syndrome），簡稱早衰症。 早衰症是一種極端罕見的 遺傳性疾病 ，其患者身體的 老化 過程十分快速。 而罹患此病孩童的年齡很少超過13歲，大約每八百萬個新生兒之中就有一位得到此疾。
program publications | The Progeria Research Foundation
This publication utilized the following Progeria Research Foundation programs: PRF Grant-Funded Program; Cell and Tissue Bank; Follow this link to obtain free full text of the article.
Progeria - StatPearls - NCBI Bookshelf - National Center for ...
Werner syndrome, also known as adult progeria, is a rare autosomal recessive condition that begins in late adolescence or early adulthood and leads to early aging.
2013年10月26日 · Progeria is also known as Hutchinson-Gilford Progeria Syndrome (HGPS). It was first described in 1886 by Dr. Jonathan Hutchinson and in 1897 by Dr. Hastings Gilford. Progeria is a rare, fatal, “premature aging” syndrome. It’s called a syndrome because all the children have very similar symptoms that “go together”.
Progeria: A rare genetic premature ageing disorder - PMC
Progeria is characterized by clinical features that mimic premature ageing. Although the mutation responsible for this syndrome has been deciphered, the mechanism of its action remains elusive. Progeria research has gained momentum particularly in ...
Progeria Related Publications - The Progeria Research Foundation
This publication utilized the following Progeria Research Foundation programs: PRF Grant-Funded Program; Cell and Tissue Bank; Follow this link to obtain free full text of the article.
Molecular insights into the premature aging disease progeria
Hutchinson–Gilford progeria syndrome (HGPS) is an extremely rare sporadic autosomal-dominant genetic disorder affecting 1 in 4–8 million newborns and displays phenotypic features of premature aging (Ghosh and Zhou 2014; Gordon et al. 2014). Children with HGPS appear normal at birth but start to exhibit many distinctive clinical features ...
An Encouraging Progress Report on the Treatment of Progeria …
2014年5月2日 · Two canonical examples are the Werner syndrome and the Hutchinson-Gilford Progeria Syndrome (HGPS). In both disorders, atherosclerosis is a particularly striking feature, causing the majority of deaths, usually via a myocardial infarction (although cancer is also a common cause of death in Werner syndrome, a later-onset disorder).
Molecular insights into the premature aging disease progeria
Hutchinson–Gilford progeria syndrome (HGPS) is an extremely rare premature aging disease presenting many features resembling the normal aging process. HGPS patients die before the age of 20 years due to cardiovascular problems and heart failure.
Progeria: a rare genetic premature ageing disorder - PubMed
Progeria is characterized by clinical features that mimic premature ageing. Although the mutation responsible for this syndrome has been deciphered, the mechanism of its action remains elusive. Progeria research has gained momentum particularly in the last two decades because of the possibility of r …