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首页> 外文期刊>Seminars in Thrombosis and Hemostasis >Gene Variations in the Protein C and Fibrinolytic Pathway: Relevance for Severity and Outcome in Pediatric Sepsis
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Gene Variations in the Protein C and Fibrinolytic Pathway: Relevance for Severity and Outcome in Pediatric Sepsis

机译:蛋白C和纤维蛋白溶解途径的基因变异:儿科败血症严重程度和结果的相关性

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摘要

The host response to infection involves complex interplays between inflammation, coagulation, and fibrinolysis. Deregulation of hemostasis and fibrinolysis are major causes of critical illness and important determinants of outcome in severe sepsis. The hemostatic responses to infection vary widely between individuals, and are in part explained by polymorphisms in genes responsible for the protein C and fibrinolytic pathway. This review gives an overview of genetic polymorphisms in the protein C and fibrinolytic pathway associated with susceptibility and severity of pediatric sepsis. In addition, genetic polymorphisms associated with adult sepsis and other pediatric thromboembolic disorders are discussed, as these polymorphisms might be candidates for future molecular genetic research in pediatric sepsis.
机译:对感染的宿主反应涉及炎症,凝血和纤维蛋白溶解之间的复杂相互作用。 止血的止血和纤维蛋白溶解是严重脓毒症患者危重疾病和重要决定因素的主要原因。 对感染的止血反应在个体之间广泛变化,并且部分是由对蛋白C和纤维蛋白溶解途径的基因中的多态性解释。 本综述概述了蛋白C和纤维蛋白溶解途径的遗传多态性概述,与儿科败血症的敏感性和严重程度相关。 此外,讨论了与成人败血症和其他小儿血栓栓塞障碍相关的遗传多态性,因为这些多态性可能是儿科败血症未来分子遗传研究的候选者。

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