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Bilateral renal vein thrombosis secondary to methylene tetrahydrofolate reductase mutation: a rare case.

作者信息

Isik Ayse, Kirbas Ismail, Kanbay Mehmet

机构信息

Department of Internal Medicine, School of Medicine , Fatih University , Ankara , Turkey.

Department of Radiology, School of Medicine , Fatih University , Ankara , Turkey.

出版信息

NDT Plus. 2010 Aug;3(4):416-7. doi: 10.1093/ndtplus/sfq049. Epub 2010 Apr 9.

DOI:10.1093/ndtplus/sfq049
PMID:25949448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4421509/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d01/4421509/9c985fdf75dc/sfq049fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d01/4421509/9c985fdf75dc/sfq049fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d01/4421509/9c985fdf75dc/sfq049fig1.jpg

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本文引用的文献

1
Renal vein thrombosis.肾静脉血栓形成
Eur J Vasc Endovasc Surg. 2007 Aug;34(2):217-23. doi: 10.1016/j.ejvs.2007.02.017. Epub 2007 Jun 1.
2
Renal vein thrombosis as a presenting symptom of multiple genetic pro-coagulant defects.肾静脉血栓形成作为多种遗传性促凝缺陷的首发症状。
Nephrol Dial Transplant. 2005 Apr;20(4):827-9. doi: 10.1093/ndt/gfh655. Epub 2005 Mar 1.
3
Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis.
高同型半胱氨酸血症、突变型亚甲基四氢叶酸还原酶（MTHFR）与遗传性易栓因素在复发性静脉血栓形成中的相互作用
Thromb Haemost. 2002 Nov;88(5):723-8.
4
Effect of MTHFR 1298A-->C and MTHFR 677C-->T genotypes on total homocysteine, folate, and vitamin B(12) plasma concentrations in kdiney graft recipients.MTHFR 1298A→C和MTHFR 677C→T基因型对肾移植受者血浆总同型半胱氨酸、叶酸和维生素B12浓度的影响。
J Am Soc Nephrol. 2000 Oct;11(10):1918-1925. doi: 10.1681/ASN.V11101918.
5
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。
Haematologica. 1999 Sep;84(9):824-8.
6
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.亚甲基四氢叶酸还原酶TT677基因型与静脉血栓形成相关，独立于FV Leiden和凝血酶原A20210突变的共存情况。
Thromb Haemost. 1998 May;79(5):907-11.