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GENETIC MARKERS FOR ASSESSING RISK OF PREMATURE BIRTH RESULTING FROM PRETERM PREMATURE RUPTURE MEMBRANES

机译:评估早产胎膜破裂导致的早产风险的遗传标记

摘要

A method to identify women who are at risk for preterm delivery due to premature rupture of membranes (PPROM) is provided. The method entails detecting the presence of SERPINH1 gene variants that express low levels of the gene product, heat shock protein Hsp47. The occurrence of a T (rather than C) at a single nucleotide polymorphism (SNP) site at position −656 of the SERPINH1 gene promoter, together with the absence of a 12 base pair deletion at positions −694 to −683 of the promoter, result in an increased risk of PPROM. The method enables medical professionals to identify those at risk, and to provide suitable therapeutic intervention.
机译:提供了一种识别因胎膜早破而处于早产风险中的妇女的方法(PPROM)。该方法需要检测表达低水平基因产物热激蛋白Hsp47的SERPINH1基因变异体的存在。在SERPINH1基因启动子的-656位单核苷酸多态性(SNP)位点出现T(而非C),并且在启动子的-694至-683位不存在12个碱基对的缺失,导致PPROM的风险增加。该方法使医学专业人员能够识别有风险的人,并提供适当的治疗干预。

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