早期识别高凝症状以预防不良健康结果

I. Grewal, Omar Elsemary, Saifullah Nasim, Ameer Almullahassani
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摘要

Leiden因子是一种遗传性疾病,导致凝血因子V和Va的卵裂位点消除。这增加了患者发生凝血事件的风险,如中风。由于缺乏筛查措施,因子V莱顿经常被忽视。我们的病例报告概述了一位中风患者,在进一步的基因检测显示因子V Leiden之前,诊断测试没有异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early Recognition of Signs of Hypercoagulability to Prevent Adverse Health Outcomes
Factor V Leiden is a genetic disorder that results in the elimination of the cleavage site on the clotting factor V and Va. This increases the risk for clotting events, such as a stroke, in affected individuals. Factor V Leiden is often overlooked due to a lack of screening measures. Our case report outlines a patient who suffered from a stroke with no abnormalities on diagnostic testing until further genetic testing revealed Factor V Leiden.
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