Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome

被引：6
|
作者：
Sipahi, T
Duru, F
Yarah, N
Akar, N
机构：
[1] Dr Sami Ulus Childrens Hosp, Dept Paediat Haematol, Ankara, Turkey
[2] Ankara Univ, Fac Med, Dept Paediat Mol Genet, TR-06100 Ankara, Turkey
[3] Hosdere Caddesi, Ankara, Turkey
来源：
EUROPEAN JOURNAL OF PEDIATRICS | 2001年 / 160卷 / 03期
关键词：
D O I：
10.1007/PL00008425
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页码：198 / 198
页数：1
相关论文
共 50 条
  • [1] Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome
    Tansu Sipahi
    Feride Duru
    Nese Yaralı
    Nejat Akar
    European Journal of Pediatrics, 2001, 160 : 198 - 198
  • [2] Budd-Chiari Syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene
    Öner, AF
    Arslan, S
    Çaksen, H
    Ceylan, A
    THROMBOSIS AND HAEMOSTASIS, 1999, 82 (04) : 1366 - 1367
  • [3] Idiopathic Budd-Chiari syndrome in a patient with homozygous Factor V Leiden and heterozygous factor II G20210A mutations
    De Stefano, V
    Madonna, P
    Giannino, A
    Coppola, A
    Cerbone, AM
    Pauciullo, P
    Di Minno, G
    THROMBOSIS RESEARCH, 2000, 100 (06) : 567 - 568
  • [4] Risk of Budd-Chiari Syndrome Associated with Factor V Leiden and G20210A Prothrombin Mutation: A Meta-Analysis
    Zhang, Peijin
    Zhang, Jing
    Sun, Guixiang
    Gao, Xiuyin
    Wang, Hui
    Yan, Wenjun
    Xu, Hao
    Zu, Maoheng
    Ma, He
    Wang, Wei
    Lu, Zhaojun
    PLOS ONE, 2014, 9 (04):
  • [5] Associations of Coagulation Factor V Leiden and Prothrombin G20210A Mutations With Budd-Chiari Syndrome and Portal Vein Thrombosis: A Systematic Review and Meta-analysis
    Qi, Xingshun
    Ren, Weirong
    De Stefano, Valerio
    Fan, Daiming
    CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2014, 12 (11) : 1801 - U267
  • [6] Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene
    Bucciarelli, P
    Franchi, F
    Alatri, A
    Bettini, P
    Moia, M
    THROMBOSIS AND HAEMOSTASIS, 1998, 79 (02) : 445 - 446
  • [7] The factor V Leiden and prothrombin G20210A mutations in Kirghiz population
    Gurgey, A
    Kudayarov, DK
    Tuncer, M
    Parlak, H
    Altay, C
    THROMBOSIS AND HAEMOSTASIS, 2000, 84 (02) : 356 - 356
  • [8] Compound heterozygosity for factor V and methylenetetrahydrofolate reductase mutations in a patient with Budd-Chiari syndrome
    Otrock, ZK
    Sharara, AI
    Mahfouz, RAR
    Taher, AT
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2006, 21 (04) : 782 - 783
  • [9] Purpura fulminans in a child with combined heterozygous prothrombin G20210A and factor V Leiden mutations
    Özbek, N
    Ataç, FB
    Verdi, H
    Kayiran, SM
    ANNALS OF HEMATOLOGY, 2003, 82 (02) : 118 - 120
  • [10] Purpura fulminans in a child with combined heterozygous prothrombin G20210A and factor V Leiden mutations
    N. Özbek
    F. B. Ataç
    H. Verdi
    S. M. Kayıran
    Annals of Hematology, 2003, 82 : 118 - 120
12345