Preimplantation Genetic Diagnosis

Q4 Medicine
Elitza Markova-Car, K. Pavelić
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引用次数: 0

Abstract

Preimplantation genetic diagnosis (PGD) or preimplantation genetic screening (PGS) is an early form of prenatal diagnosis which allows that, before the pregnancy has begun, embryos can be tested for genetic disorders. 1 The rationale behind the method lies in the removal of cells from early embryos and genetic analysis of these cells before being transferred to the uterus. This procedure offers an advantage for those couples having genetic disorders whose offspring has an increased risk of a specific genetic condition by helping in the delivery of a healthy baby or prevention of repeated spontaneous abortions. 2 As a result, PGS has developed as a valuable tool for enhancing pregnancy success with assisted reproductive technologies. 3 In fact, PGD may possibly be suggested for any disorder for which molecular testing can be performed.
胚胎植入前遗传学诊断
植入前遗传学诊断(PGD)或植入前遗传学筛查(PGS)是产前诊断的一种早期形式,它允许在怀孕开始之前对胚胎进行遗传疾病检测。该方法背后的原理在于从早期胚胎中取出细胞,并在将这些细胞转移到子宫之前对其进行遗传分析。对于那些有遗传病的夫妇,他们的后代患某种特定遗传病的风险增加,这种程序通过帮助分娩健康婴儿或防止反复自然流产,为他们提供了一个优势。因此,PGS已发展成为辅助生殖技术提高妊娠成功率的宝贵工具。事实上,PGD可能被建议用于任何可以进行分子检测的疾病。
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来源期刊
Donald School Journal of Ultrasound in Obstetrics and Gynecology
Donald School Journal of Ultrasound in Obstetrics and Gynecology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.50
自引率
0.00%
发文量
32
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