早期识别高凝症状以预防不良健康结果

Clinical Case Studies and Reports Pub Date : 2023-05-23 DOI:10.59657/2837-2565.brs.23.036

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。

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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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Clinical Case Studies and Reports

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