土耳其儿童白血病患者的因子V Leiden和凝血酶原20210A突变

Leukemia Research and Treatment Pub Date : 2012-01-01 Epub Date: 2012-02-16 DOI:10.1155/2012/250432
Dilara Fatma Akın, Kadir Sipahi, Tuğba Kayaalp, Yonca Eğin, Serpil Taşdelen, Emin Kürekçi, Ustün Ezer, Nejat Akar
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引用次数: 6

摘要

本研究旨在确定土耳其白血病儿童中v1691 G-A因子和PT 20210 G-A突变的患病率。我们对135名患有这些突变的儿童白血病患者进行了基因分型。135例患者中有11例(8%)为FV 1691 G-A突变的杂合子。7例(5.1%)患者携带PT 20210 G-A杂合突变。在135例患者中,只有3例发生血栓事件,没有一例具有这两种突变,这在土耳其人群中很常见。我们的研究结果与以往的报道相比存在争议,有待进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factor V Leiden and Prothrombin 20210A Mutations among Turkish Pediatric Leukemia Patients.

This study was undertaken to determine the prevalence of the Factor V 1691 G-A and PT 20210 G-A mutations in Turkish children with leukemia. We genotyped 135 pediatric leukemia patients with for these mutations. Eleven (8%) of the 135 patients were heterozygous for the FV 1691 G-A mutation. Seven (5,1%) of the patients carried the PT 20210 G-A heterozygous mutation. Of the 135 patients, only three had thrombotic event, none of which had these two mutations, which is common in Turkish population. Our findings revealed a controversial compared to the previous reports, which needs further investigation.

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