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Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.

作者信息

Bucciarelli P, Franchi F, Alatri A, Bettini P, Moia M

出版信息

Thromb Haemost. 1998 Feb;79(2):445-6.

PMID:9493607
Abstract
摘要

相似文献

1
Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.一名凝血酶原基因G20210A突变杂合子患者的布加综合征
Thromb Haemost. 1998 Feb;79(2):445-6.
2
Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.一名同时携带因子V莱顿突变和凝血酶原基因G20210A突变的杂合子患者发生布加综合征。
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3
JAK2V617F and prothrombin G20210A gene mutations in a patient with Budd-Chiari syndrome and essential thrombocythemia.患者患有布加综合征和特发性血小板增多症，存在 JAK2V617F 和凝血酶原 G20210A 基因突变。
Clin Appl Thromb Hemost. 2010 Aug;16(4):472-4. doi: 10.1177/1076029609332110. Epub 2009 Feb 16.
4
Relations of Budd-Chiari syndrome to prothrombin gene mutation.
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Portal and mesenteric venous thrombosis in a patient heterozygous for the 20210 A allele of the prothrombin gene.一名凝血酶原基因20210A等位基因杂合子患者发生门静脉和肠系膜静脉血栓形成。
Haematologica. 1998 Dec;83(12):1129-30.
6
Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.一名患有布加综合征的儿童存在因子V莱顿突变和凝血酶原G20210A突变的复合杂合性。
Eur J Pediatr. 2001 Mar;160(3):198. doi: 10.1007/pl00008425.
7
Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele.
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Acute Budd-Chiari syndrome during pregnancy: surgical treatment and orthotopic liver transplantation with successful completion of the pregnancy.妊娠期急性布加综合征：手术治疗及原位肝移植并成功完成妊娠
Liver Transpl. 2003 Sep;9(9):976-9. doi: 10.1053/jlts.2003.50134.
9
Budd-Chiari syndrome in a patient heterozygous for the point mutation C20221T of the prothrombin gene.一名凝血酶原基因C20221T点突变杂合子患者的布加综合征
J Thromb Haemost. 2003 Apr;1(4):852-3. doi: 10.1046/j.1538-7836.2003.t01-2-00115.x.
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Idiopathic Budd-Chiari syndrome in a patient with homozygous Factor V Leiden and heterozygous Factor II G20210A mutations.一名患有纯合子因子V莱顿突变和杂合子因子II G20210A突变的患者的特发性布加综合征。
Thromb Res. 2000 Dec 15;100(6):567-8. doi: 10.1016/s0049-3848(00)00355-8.

引用本文的文献

1
A Novel Culprit in a Patient with Budd-Chiari Syndrome.布加综合征患者的一个新病因
Case Rep Gastroenterol. 2021 May 25;15(2):470-474. doi: 10.1159/000516210. eCollection 2021 May-Aug.
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
Concomitant homozygosity for the prothrombin gene variant with mild deficiency of antithrombin III in a patient with multiple hepatic infarctions: a case report.
一名患有多发性肝梗死患者同时存在凝血酶原基因变异纯合子和抗凝血酶III轻度缺乏：病例报告
J Med Case Rep. 2010 Apr 29;4:122. doi: 10.1186/1752-1947-4-122.
4
Prothrombin 20210G/A mutation in two patients with mesenteric ischemia.
Dig Dis Sci. 1999 Sep;44(9):1910-3. doi: 10.1023/a:1018867311839.