Pathare A, Alkindi S, Albalushi T, Bayoumi R, Dennison D, Muralitharan S
Department of Haematology, College of Medicine, Sultan Qaboos University Hospital, Muscat, Sultante of Oman.
Clin Lab Haematol. 2004 Apr;26(2):143-6. doi: 10.1111/j.1365-2257.2004.00585.x.
Hyperhomocysteinemia is known to be associated with arterial occlusive vascular disease and venous thrombosis. Here, we report a young ethnic Omani patient with recurrent venous thrombosis who was found to be heterozygous for 677C-T mutation in the methyltetrahydrofolate reductase (MTHFR) enzyme. Moderate hyperhomocystenemia was also observed, in the presence of normal red cell folate and serum B12 levels. No other documented marker of hereditary thrombophilia could be demonstrated in this patient, in spite of extensive investigation on multiple occasions.
高同型半胱氨酸血症已知与动脉闭塞性血管疾病和静脉血栓形成有关。在此,我们报告一名年轻的阿曼族患者,该患者反复发生静脉血栓形成,被发现甲基四氢叶酸还原酶(MTHFR)酶的677C-T突变呈杂合状态。尽管红细胞叶酸和血清B12水平正常,但也观察到中度高同型半胱氨酸血症。尽管多次进行了广泛检查,但该患者未发现其他已记录的遗传性血栓形成倾向标志物。