In vitro fertilization as an option for couples with genetic disorders.

IF 1.8 Q3 OBSTETRICS & GYNECOLOGY
F Yudha Christianti, Legiran Legiran
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引用次数: 0

Abstract

Errors in human DNA may cause genetic disorders. Technological developments have raised hopes for reducing the risks of genetic inheritance among married couples who have a history of such disorders. Among the developments in reproductive health technology that reduce those risks is the in vitro fertilization (IVF) process. This review aimed to describe the current strategies using IVF and preimplantation genetic testing (PGT), which would be effective for couples with genetic disorders to have healthy offspring. The literature review included full-text, open-access research articles from ScienceDirect, PubMed, and Google Scholar that were published between 2013 and 2023, with 65 articles obtained from various journals. The keywords were "in vitro fertilization," "reproductive genetic disorders," "PGT-A," "PGT-M," "PGT-SR," and "oocyte donor." A total of 46 articles were selected as the most relevant to the review topic, and the results show that the IVF process can be an option for couples with a history of genetic disorders. Several additional procedures can be performed following IVF, such as oocyte donation and PGT, to help couples who want to have offspring without transmitting their genetic disorders. IVF can be an option for couples who have or carry genetic disorders. With IVF, couples can undertake several procedures such as oocyte donation and PGT for aneuploidy, monogenic disorders, or structural rearrangement.

将体外受精作为患有遗传性疾病的夫妇的一种选择。
人类 DNA 中的错误可能导致遗传疾病。技术的发展为降低有遗传病史的已婚夫妇的遗传风险带来了希望。在生殖健康技术的发展中,体外受精(IVF)过程可以降低这些风险。本综述旨在描述目前使用体外受精和植入前基因检测(PGT)的策略,这些策略将有效帮助有遗传疾病的夫妇生育健康的后代。文献综述包括ScienceDirect、PubMed和Google Scholar上发表于2013年至2023年间的全文开放存取研究文章,其中65篇文章来自不同期刊。关键词为 "体外受精"、"生殖遗传疾病"、"PGT-A"、"PGT-M"、"PGT-SR "和 "卵细胞捐赠者"。结果显示,试管婴儿过程可以成为有遗传病史的夫妇的一种选择。体外受精后还可以进行一些额外的程序,如卵细胞捐赠和PGT,以帮助那些希望在不遗传其遗传疾病的情况下生育后代的夫妇。对于患有或携带遗传疾病的夫妇来说,体外受精也是一种选择。通过体外受精,夫妇可以进行多项程序,如卵细胞捐献和非整倍体、单基因遗传病或结构重排的 PGT。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.30
自引率
0.00%
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