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Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.

作者信息

Zawadzki C, Gaveriaux V, Trillot N, Bauters A, Watel A, Alhenc-Gelas M, Preudhomme C, Jude B

出版信息

Thromb Haemost. 1998 Dec;80(6):1027-8.

PMID:9869179
Abstract
摘要

相似文献

1
Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.凝血酶原基因中与严重静脉血栓形成疾病相关的纯合子G20210A转变：一个法国家庭中的两例病例。
Thromb Haemost. 1998 Dec;80(6):1027-8.
2
Application of the TaqMan-PCR for genotyping of the prothrombin G20210A mutation and of the thermolabile methylenetetrahydrofolate reductase mutation.TaqMan聚合酶链反应在凝血酶原G20210A突变和不耐热亚甲基四氢叶酸还原酶突变基因分型中的应用。
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The VITA project: prothrombin G20210A mutation and venous thromboembolism in the general population.VITA项目：普通人群中的凝血酶原G20210A突变与静脉血栓栓塞
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Thrombosis-associated gene variants in sickle cell anemia.
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Thromb Haemost. 1998 Dec;80(6):1028-9.
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C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients.亚甲基四氢叶酸还原酶基因中的C677T替换作为特定患者静脉血栓形成和动脉疾病的危险因素。
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A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.一名年轻女性中凝血酶原20210A变异的纯合状态作为孕期深静脉血栓形成的原因
Eur J Haematol. 2000 Jul;65(1):80-1. doi: 10.1034/j.1600-0609.2000.9l140.x.
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A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667t mutations, but belonging to an asymptomatic family.一名患有静脉血栓形成的男孩，为凝血因子V莱顿、凝血酶原G20210A和亚甲基四氢叶酸还原酶C667t突变的纯合子，但来自一个无症状家族。
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[C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism].[俄罗斯中部地区静脉血栓形成患者亚甲基四氢叶酸还原酶基因C677T突变与肺动脉血栓栓塞高风险相关]
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Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischemic optic neuropathy and ischemic stroke.遗传性与雌激素诱导的血栓形成倾向的相互作用：缺血性视神经病变和缺血性中风的可能病因
Thromb Haemost. 2001 Feb;85(2):256-9.

引用本文的文献

1
Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review.凝血酶原G20210A基因突变所致复发性深静脉血栓形成和肺栓塞：病例报告及文献复习
J Investig Med High Impact Case Rep. 2022 Jan-Dec;10:23247096211058486. doi: 10.1177/23247096211058486.
2
Bilateral Superficial Femoral Artery Thrombosis in a 15-Year-Old Caucasian Male with Homozygous Prothrombin G20210A Genotype and Associated Antiphospholipid Syndrome.一名15岁白种男性，患有纯合子凝血酶原G20210A基因型及相关抗磷脂综合征，出现双侧股浅动脉血栓形成
Int J Angiol. 2016 Dec;25(5):e100-e105. doi: 10.1055/s-0035-1548557. Epub 2015 Mar 23.
3
Phenotypic Heterogeneity in Patients with Homozygous Prothrombin 20210AA Genotype. A paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology.
纯合子凝血酶原20210AA基因型患者的表型异质性。一篇来自2005年威廉·博蒙特医院分子病理学研讨会的论文。
J Mol Diagn. 2006 Sep;8(4):420-5. doi: 10.2353/jmoldx.2006.060014.