生殖医学的基因组方面。

IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Clinical and Experimental Reproductive Medicine-CERM Pub Date : 2024-06-01 Epub Date: 2024-01-24 DOI:10.5653/cerm.2023.06303
Minyeon Go, Sung Han Shim
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引用次数: 0

摘要

不孕不育是一种复杂的疾病,其特点是遗传异质性极强,再加上各种环境因素的影响。虽然也有例外情况,但与不孕不育有关的个体遗传和基因组变异通常很少见,而且往往具有家族特异性,可作为易感因素而非直接病因。因此,即使在现代基因组时代,确定不孕不育的原因并根据这些因素制定预防和治疗策略仍然是一项具有挑战性的任务。在这篇综述中,我们首先探讨了与不孕症相关的基因和基因组变异,随后根据基因组分析技术的发展总结了胚胎植入前基因检测的概念和方法。
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Genomic aspects in reproductive medicine.

Infertility is a complex disease characterized by extreme genetic heterogeneity, compounded by various environmental factors. While there are exceptions, individual genetic and genomic variations related to infertility are typically rare, often family-specific, and may serve as susceptibility factors rather than direct causes of the disease. Consequently, identifying the cause of infertility and developing prevention and treatment strategies based on these factors remain challenging tasks, even in the modern genomic era. In this review, we first examine the genetic and genomic variations associated with infertility, and subsequently summarize the concepts and methods of preimplantation genetic testing in light of advances in genome analysis technology.

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