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Prothrombin gene mutation in Budd-Chiari syndrome-The first case report from India.

作者信息

Jain Abhinav, Shukla Akash

机构信息

Department of Gastroenterology, Seth G S Medical College and K E M Hospital, Parel, Mumbai, 400 012, India.

出版信息

Indian J Gastroenterol. 2018 Mar;37(2):174-175. doi: 10.1007/s12664-018-0845-x. Epub 2018 Apr 4.

DOI:10.1007/s12664-018-0845-x
PMID:29616413
Abstract
摘要

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本文引用的文献

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Budd-Chiari syndrome/hepatic venous outflow tract obstruction.布加综合征/肝静脉流出道梗阻。
Hepatol Int. 2018 Feb;12(Suppl 1):168-180. doi: 10.1007/s12072-017-9810-5. Epub 2017 Jul 6.
2
Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis.风险与因子 V 莱顿和 G20210A 凝血酶原突变相关的布加氏综合征：荟萃分析。
PLoS One. 2014 Apr 22;9(4):e95719. doi: 10.1371/journal.pone.0095719. eCollection 2014.
3
Hereditary and Acquired Thrombophilia in Splanchnic Vein Thrombosis: A Single-Center Experience.
内脏静脉血栓形成中的遗传性和获得性易栓症：单中心经验
Clin Appl Thromb Hemost. 2015 Sep;21(6):521-6. doi: 10.1177/1076029613511520. Epub 2013 Nov 19.
4
Clinical and prothrombotic profile of hepatic vein outflow tract obstruction.肝静脉流出道梗阻的临床和血栓前状态
Indian J Pediatr. 2014 May;81(5):434-40. doi: 10.1007/s12098-013-1131-7. Epub 2013 Jul 25.
5
Changing spectrum of Budd-Chiari syndrome in India with special reference to non-surgical treatment.印度布加综合征的变化谱，特别提及非手术治疗
World J Gastroenterol. 2008 Jan 14;14(2):278-85. doi: 10.3748/wjg.14.278.
6
Low frequency of factor V Leiden and prothrombin G20210A mutations in patients with hepatic venous outflow tract obstruction in northern India: a case-control study.印度北部肝静脉流出道梗阻患者中因子V莱顿突变和凝血酶原G20210A突变的低发生率：一项病例对照研究。
Indian J Gastroenterol. 2005 Sep-Oct;24(5):211-5.
7
Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India.布加综合征和门静脉血栓形成中的遗传性血栓前缺陷：一项来自印度北部的研究。
Am J Clin Pathol. 2004 Jun;121(6):844-7. doi: 10.1309/F2U1-XBV4-RXYU-AYG0.
8
Hereditary thrombophilia as a cause of Budd-Chiari syndrome: a study from Western India.遗传性血栓形成倾向作为布加综合征的一个病因：来自印度西部的一项研究。
Hepatology. 2001 Oct;34(4 Pt 1):666-70. doi: 10.1053/jhep.2001.27948.
9
G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men.凝血酶原基因G20210A突变与一大群美国男性发生心肌梗死、中风和静脉血栓形成的风险
Circulation. 1999 Mar 2;99(8):999-1004. doi: 10.1161/01.cir.99.8.999.
10
A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.凝血酶原基因3'非翻译区的一种常见基因变异与血浆凝血酶原水平升高及静脉血栓形成增加有关。
Blood. 1996 Nov 15;88(10):3698-703.