血栓友病的综合性审查:病理生理学,患病率,危险因素和分子诊断
Reham Altwayan1, Huseyin Tombuloglu2, Galyah Alhamid2
1Department of Genetics Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, 31441 Dammam, Saudi Arabia; Master Program of Biotechnology, Institute for Research and Medical Consultations, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
概括
血栓ophilia,一个凝血障碍,每年影响数百万. 这篇评论详细介绍了其原因,遗传突变和生活方式等风险以及诊断需求.
科学领域:
- 血液学 血液学 血液学
- 遗传学 是一个遗传学.
- 流行病学 流行病学
背景情况:
- 血栓ophilia是一个严重的,诊断不足的疾病,导致不适当的血液凝固,与美国显著的死亡率.
- 它源于遗传因素 (例如,V Leiden因素) 和环境影响 (例如,肥胖,癌症).
- 风险因素包括年龄,家族病史,怀孕和SARS-CoV-2感染.
研究的目的:
- 为提供有关血栓友爱症的最新系统审查.
- 综合有关病理生理学,流行病学,风险因素和诊断的证据.
- 为了指导临床诊断和管理.
主要方法:
- 系统的文献审查.
- 临床和分子证据的综合.
- 对凝血级联和遗传突变流行率的分析.
主要成果:
- 血栓ophilia涉及复杂的遗传环境相互作用.
- 遗传突变的发病率在不同种群之间有很大的差异.
- 现有的诊断方法需要提高成本效益和广泛应用.
结论:
- 准确的诊断和对血栓友爱症的治疗至关重要.
- 需要对强大的查方法进行进一步的研究.
- 本综述为医疗保健专业人员提供了一个全面的资源.
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