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Genetic and epigenetic variations associated with idiopathic recurrent pregnancy loss

机译:与特发性反复妊娠流产有关的遗传和表观遗传变异

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摘要

Recurrent pregnancy loss (RPL) is a reproductive disorder defined as two or more successive and spontaneous pregnancy losses (before 20 weeks of gestation), which affects approximately 1–2% of couples. At present, the causes of RPL remain unknown in a considerable number of cases, leading to complications in treatment and high levels of stress in couples. Idiopathic recurrent pregnancy loss (iRPL) has become one of the more complicated reproductive problems worldwide due to the lack of information about its etiology, which limits the counseling and treatment of patients. For that reason, iRPL requires further study of novel factors to provide scientific information for determining clinical prevention and targeted strategies. The aim of this study is to describe the most recent and promising progress in the identification of potential genetic and epigenetic risk factors for iRPL, expanding the genetic etiology of the disease.
机译:复发性流产(RPL)是一种生殖疾病,定义为两次或两次以上连续且自发的流产(在妊娠20周之前),影响大约1-2%的夫妇。目前,在许多情况下,RPL的病因仍不明,导致治疗并发症和夫妻压力很大。由于缺乏病因学信息,特发性反复妊娠流产(iRPL)已成为全球范围内最复杂的生殖问题之一,这限制了患者的咨询和治疗。因此,iRPL需要进一步研究新因素,以便为确定临床预防措施和靶向策略提供科学信息。这项研究的目的是描述在鉴定iRPL的潜在遗传和表观遗传风险因素方面的最新和有希望的进展,从而扩大该疾病的遗传病因。

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