The meaning of FACTOR V LEIDEN is a point mutation producing an abnormal version of factor V that is resistant to inactivation and causes prolonged clotting of blood.
遗传阻断导读:Factor V Leiden易栓症是一种儿科疾病。佳学基因对Factor V Leiden易栓症的发生进行了基因解码,并将之收入《人的基因序列变化与人体疾病表征》中,便于医生选择和使用,进行Factor V Leiden易栓症遗传阻断,也便于患者更好地进行治疗和健康管理。
Early epidemiologic data suggested that an abnormally low anticoagulant response to APC, termed "acti- vated protein C resistance (APC-R)," was familial, with an auto- somal dominant or semidominant inheritance pattern.7 Factor Va isolated from APC-R patient plasma was resistant to inactivation ...
Factor V Leiden (FV Leiden) and AV Graft thrombosis(AVG) in children with end stage renal disease(ESRD). 16851997 Abstracts The American Pediatric Society and The Society for Pediatric Researchdoi:10.1203/00006450-199704001-01704Yatin Shah
FactorVLeiden易栓症是英文factor V Leiden thrombophilia的中文翻译。这一疾病又叫做facio-scapulo-humeral dystrophyfacioscapulohumeral atrophyfacioscapulohumeral type progressive muscular dystrophyfacioscapuloperoneal muscular dystrophyFSH muscular dystrophyFSHDmuscular dystrophy, facioscapulohumeral;。该病是一种基因...
factor-V Leiden A common mutation of coagulation factor-V gene, which is found in 3 to 8% of Caucasians, and results in resistance to activated C protein and an increased risk in deep-vein and other thromboses. Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved....
Professor at Leiden University, the Netherlands in 1998. shawprize.org 于1990年至1994年间,她曾在不同学院从事博士后研究,其中包括哈佛史密森天体物理中心、加州大学柏 克莱分校和斯坦福大学,1994年被委任为哈佛大学助理教授及1998年为 荷 兰 莱 顿 大 学教 授。 shawprize.org [...] invited the Secret...
(11,16,21–23). The inheritance pattern is autosomal-dominant butpenetranceis considered incomplete because most affected patients who present with clinical thrombosis are predisposed by additional inherited and/or acquired prothrombotic risk factors. The racial predilection of this mutation is also ...
Type 2A is mainly inherited as autosomal dominant, but recessive inheritance has also been described. Patients with type 2A vWD have normal to low vWF:Ag levels with disproportionately lower vWF:RCo and an abnormal multimer pattern characterized by loss of high-molecular-weight multimers. The reduc...
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