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遗传性血栓形成倾向突变对一名患有抗磷脂综合征和系统性红斑狼疮青少年的影响。

Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosus.

作者信息

Higginbotham E A, Zimmerman S A, Howard T A, Schanberg L, Kredich D, Ware R E

机构信息

Medicine-Pediatric Residency Training Program, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

J Rheumatol. 2001 Feb;28(2):370-2.

Abstract

Thrombophilia can result from either inherited or acquired conditions. We describe a teenager who developed extensive thrombosis requiring aggressive and prolonged anticoagulation. Laboratory evaluation revealed an acquired lupus anticoagulant, consistent with the antiphospholipid antibody syndrome (APS). DNA analysis revealed inherited thrombophilic mutations in the factor V and methylene tetrahydrofolate reductase genes. We believe that the combination of inherited and acquired hypercoagulable conditions affected her therapeutic response to anticoagulant therapy. Inherited thrombophilic DNA mutations may contribute to the hypercoagulability observed in patients with acquired thrombophilic conditions such as APS and systemic lupus erythematosus.

摘要

血栓形成倾向可由遗传性或后天性疾病引起。我们描述了一名青少年,其发生了广泛的血栓形成,需要积极且长期的抗凝治疗。实验室检查发现存在后天获得性狼疮抗凝物,符合抗磷脂抗体综合征(APS)。DNA分析显示在因子V和亚甲基四氢叶酸还原酶基因中存在遗传性血栓形成倾向突变。我们认为,遗传性和后天获得性高凝状态的共同作用影响了她对抗凝治疗的反应。遗传性血栓形成倾向DNA突变可能导致在患有后天性血栓形成倾向疾病(如APS和系统性红斑狼疮)的患者中观察到的高凝状态。

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