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Increased chromosome abnormalities in human preimplantation embryos afterin-vitro fertilization in patients with recurrent miscarriage

机译:反复流产患者体外受精后植入前胚胎的染色体异常增加

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Recurrent miscarriage is a pathological condition induced by maternal and embryonic causes. This paper describes a prospective study to determine the real incidence of aneuploidy for autosomes 13, 16, 18, 21, 22, and gonosomes in preimplantation human embryos obtained from patients with recurrent pregnancy loss after ovarian stimulation in an IVF-ET programme, Our results indicate that aneuploidy for the chromosomes analysed are abnormally higher in embryos obtained after IVF from recurrent abortion patients (58%) compared to non-recurrent abortion patients undergoing IVE Furthermore, monosomies are six times more frequent than trisomies (47:8) in preimplantation embryos from recurrent abortion patients. Based on the present study, preimplantation genetic diagnosis (PGD) of embryos obtained from patients with recurrent miscarriage could prove advantageous in diagnosing abnormal embryos and selecting normal embryos for transfer.
机译:反复流产是由母体和胚胎原因引起的病理状况。本文描述了一项前瞻性研究,以确定在IVF-ET计划中从卵巢刺激后复发性流产的患者获得的植入前人类胚胎中常染色体13、16、18、21、22和性体的非整倍体的实际发生率,我们的结果指出,与接受IVE的非反复流产患者相比,从反复流产患者进行IVF后获得的胚胎中分析的染色体的非整倍性异常高(58%)。此外,在植入前的胚胎中,单倍体的发生频率是三倍体(47:8)的六倍。来自反复流产的患者。基于本研究,从反复流产患者获得的胚胎的植入前遗传学诊断(PGD)可以证明在诊断异常胚胎和选择正常胚胎进行移植方面具有优势。

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