疾病中文名:早老症 疾病英文名:Hutchinson Gilford progeria syndrome 别名:progeria 患病率:<1 / 1 000 000 遗传方式:常染色体显性 病因 Progeria(早老症)患者在儿童时期会有提早老化的现象发生,又称为Hutchinson - Gilford progeria syndrome。早老症最早是在...
早年衰老综合症(Hutchinson-Gilford Progeria syndrome),简称早衰症。1886年Hutchinson首例报道,1897年Guilford进一步描述,所以也称Hutchinson-Gilford综合征.后来文献中称为HGPS.流行病学调查显示,美国本病的发病率为1/800万,男女之比为1.5:1,97%为白色人种.早衰症是一种极端罕见的先天遗传性疾病,其患者身体的老化过程...
Hutchinson-Gilford-Progeria综合征(HGPS)是一种节段性早衰性疾病,可导致患者因心血管功能不全而在青少年早期死亡。虽然HGPS不能完全再现正常的衰老过程,但它确实与正常的衰老过程有许多相似之处,患者还发展为心血管疾病、脱发、骨关节异常和脂肪变化。因此,毫不奇怪的是,随着医生和科学家寻找治疗HGPS的方法,他们已经...
hutchinson-gilfordprogeria网络早衰症 网络释义 1. 早衰症 ...·安德鲁斯(DeanAndrews)患有一种罕见的早衰症(Hutchinson-Gilfordprogeria),他的身体衰老速度是正常人的8倍。spzx.foods1.com|基于2个网页© 2025 Microsoft 隐私声明和 Cookie 法律声明 广告 帮助 反馈...
Progeria(Hutchinson-Gilford Syndrome)早衰症 Othernames:-Hutchinson–Gilfordprogeriasyndrome,Hutchinson–Gilfordsyndrome Definition:Hutchinson-Gilfordprogeriasyndromeisagenetic conditioncharacterizedbythedramatic,rapidappearanceofagingbeginninginchildhood.Affectedchildrentypicallylooknormalatbirthandinearlyinfancy,but...
(redirected from Hutchinson Gilford Progeria Syndrome)Also found in: Thesaurus, Medical, Encyclopedia. pro·ger·i·a (prō-jîr′ē-ə) n. A rare genetic disorder of childhood that is characterized by rapid onset of the physical changes typical of old age, usually resulting in death ...
Hutchinson-Gilford Progeria SyndromeA genetic condition characterized by the dramatic, rapid appearance of aging beginning in childhood. Affected children typically look normal at birth and in early infancy, but then grow more slowly than other children and do not gain weight at the expected rate (...
Hutchinson-Gilford progeria syndrome (HGPS) is a rare pediatric genetic syndrome with incidence of one per eight million live births. The disorder is characterised by premature aging, generally leading to death at approximately 13.4 years of age. This is a follow-up study of a 9-year-old male...
Progeria, also known as Hutchinson-Gilford progeria syndrome (HGPS), is a rare genetic condition that results in a child's body aging rapidly. A mutation in the LMNA gene causes it to make an abnormal protein. When cells use this protein, called progerin, they break down more easily, whic...
Hutchinson-Gilford progeria syndrome (HGPS) is a childhood premature aging disease caused by a spontaneous point mutation in lamin A (encoded by LMNA), one... P Scaffidi,T Misteli - 《Nature Medicine》 被引量: 1186发表: 2005年 Phenotype and course of Hutchinson-Gilford progeria syndrome. BACK...