化合物杂合因子VII缺乏c.1025G>A.p.(Arg342Gln)与新的错义变体c.194C>G.p.(Ala65Gly)

IF 1.3 Q4 HEMATOLOGY
C. Gallardo, L. Wong, C. L. L. Sum, L. Goh, K. Ong
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引用次数: 0

摘要

因子VII(FVII)缺乏表现为凝血酶原时间(PT)延长和FVII活性降低。我们报告了一例无症状的60岁绅士,在使用三种不同的凝血活酶试剂时,PT和FVII凝血活性水平(FVII:C)存在差异。对基因组DNA的进一步序列分析显示,F7基因中c.1025G>A p.Arg342Gln和c.194C>G p.Ala65Gly具有双重杂合性。到目前为止,F7基因外显子2的p.Ala65Gly在FVII缺乏症患者中代表了一种新的变体,被归类为可能的致病性。计算预测工具支持对基因的有害影响。本病例报告提出了该外显子2错义变体的基因型-表型相关性和临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Compound Heterozygous Factor VII Deficiency c.1025G>A p.(Arg342Gln) With Novel Missense Variant c.194C>G p.(Ala65Gly)
Factor VII (FVII) deficiency manifests as prolonged prothrombin time (PT) and reduced FVII activity. We report a case of an asymptomatic 60-year-old gentleman with discrepancies in PT and FVII coagulant activity levels (FVII:C) on three different thromboplastin reagents used. Further sequence analysis on genomic DNA showed double heterozygosity for c.1025G>A p.Arg342Gln and c.194C>G p.Ala65Gly in the F7 gene. To date, p.Ala65Gly in exon 2 of the F7 gene represents a novel variant in patients with FVII deficiency and is classified as likely pathogenic. Computational prediction tools support a deleterious effect on the gene. The genotype-phenotype association and the clinical significance of this exon 2 missense variant is proposed in this case report.
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来源期刊
Journal of hematology
Journal of hematology HEMATOLOGY-
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