病例报告:PROS1 (p.Leu584Arg) 致病突变导致门口和上层介质静脉血栓栓塞
Peng Ding1, Yuan Zhou2, Kai-Chen Zhang1
1Department of Critical Care Medicine, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Frontiers in cardiovascular medicine
|November 30, 2023
概括
一名因PROS1基因突变而患有门静脉血栓症和S蛋白缺乏症的患者在抗凝固治疗后恢复良好. 埃诺克萨帕林和里瓦罗克萨班在治疗这种罕见的血栓友爱病例方面被证明是有效的.
科学领域:
- 遗传学 是一个遗传学.
- 血液学 血液学 血液学
- 血管医学 血管医学
背景情况:
- 静脉血栓塞栓症 (VTE) 由遗传和获得的风险因素引起.
- 与PROS1基因突变相关的自体主导蛋白S缺乏症是已知的血栓友爱风险因素.
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