Central retinal vein thrombosis associated with prothrombin 20210G/A gene variant

被引：0
|
作者：
Vayá, A
López, JM
Mira, Y
Ricart, JM
Villa, P
España-Gregori, E
Estellés, A
Aznar, J
机构：
[1] Univ Valencia, Hosp La Fe, Dept Clin Pathol, Valencia 46009, Spain
[2] Univ Valencia, Hosp La Fe, Dept Opt & Ophthalmol, Valencia 46009, Spain
[3] Univ Valencia, Hosp La Fe, Res Ctr, Valencia 46009, Spain
来源：
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS | 1999年 / 5卷 / 03期
关键词：
retinal vein thrombosis; prothrombin gene; 20210A allele;
D O I：
10.1177/107602969900500310
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
We describe a patient with central retinal vein thrombosis associated with the prothrombin gene 20210G/A. The associated risk factors and the patient's personal and family history of thrombosis are dealt with. Ln addition, the literature on the cases reported up to now is reviewed as is the prevalence of this new mutation in patients with central retinal vein thrombosis.
引用
收藏
页码：190 / 191
页数：2
相关论文
共 50 条
  • [1] Homozygous 20210G/A prothrombin gene mutation associated with bilateral iliac vein thrombosis:: A case report
    Vayá, A
    García, M
    Mira, Y
    Ferrando, F
    Villa, P
    Estellés, A
    Aznar, J
    THROMBOSIS RESEARCH, 2001, 104 (04) : 293 - 296
  • [2] Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis
    Abraham Koshy
    Mary Jeyakumari
    Annals of Hematology, 2006, 85 : 126 - 128
  • [3] Branch retinal vein occlusion associated with the 20210 G-to-A prothrombin variant
    Martínez, CP
    Martínez, JAA
    Díaz-Llopis, M
    Gregori, EE
    Menezo, JL
    Vayá, A
    EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2000, 10 (02) : 177 - 179
  • [4] Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis
    Koshy, A
    Jeyakumari, M
    ANNALS OF HEMATOLOGY, 2006, 85 (02) : 126 - 128
  • [5] Idiopathic central retinal vein occlusion in 2 siblings with the 20210 G→A prothrombin variant
    Peris-Martinez, C
    Díaz-Llopis, M
    Menezo, JL
    ARCHIVES OF OPHTHALMOLOGY, 2002, 120 (12) : 1752 - 1754
  • [6] Cerebral vein thrombosis and prothrombin gene (G20210A) mutation
    Heckmann, JG
    Tomandl, B
    Erbguth, F
    Neidhardt, B
    Zingsem, H
    Neundörfer, B
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2001, 103 (03) : 191 - 193
  • [7] The prothrombin gene G20210A variant is a risk factor for cerebral-vein thrombosis.
    Ehrenforth, S
    Junker, R
    Nabavi, DG
    Assmann, G
    Ringelstein, EB
    Scharrer, I
    Nowak-Göttl, U
    BLOOD, 1998, 92 (10) : 558A - 558A
  • [8] Prothrombin gene variant (G20210A) in a patient with cerebral venous sinus thrombosis and bilateral deep vein thrombosis
    Ortín, X
    Ugarriza, A
    Escoda, L
    Mesa, R
    MEDICINA CLINICA, 2004, 122 (04): : 158 - 158
  • [9] The mutation Ala→Val in the methylene tetrahydrofolate reductase gene and prothrombin gene variant (20210 G→A) in children with portal vein thrombosis
    Seixas, CA
    Arruda, VR
    Barbosa, HLC
    Annichino-Bizzacchi, JM
    THROMBOSIS AND HAEMOSTASIS, 1999, : 187 - 188
  • [10] Hypercoagulable state and retinal vein thrombosis: A role for factor V Leiden and the G20210 mutation of the prothrombin gene
    Albisinni, R
    Coppola, A
    Cirillo, F
    Garofano, T
    Rugiada, F
    Greco, GM
    Cerbone, AM
    Di Minno, G
    THROMBOSIS RESEARCH, 1998, 91 (03) : S94 - S95
12345