胎儿先天性心脏病(CHD)相关基因及诊断检测方法研究进展

Q4 Medicine
Junshu Xie, Kexin Zhang, Xiaohong Zhang
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引用次数: 0

摘要

先天性心脏病(CHD)是最常见的先天性畸形之一,是一种多基因疾病,与一些主要基因有关,并与环境因素有关。随着科学技术的进步,遗传模式的研究和检测方法的研究都取得了进步。了解每个基因如何参与正常和病理解剖是冠心病研究的重要目标。我们对检测方法和冠心病相关基因的研究进展进行了综述,以期为冠心病产前诊断提供一些启示,并希望将来能够实现对冠心病基因水平的干预和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancement in research on genes associated with fetal congenital heart disease (CHD) and diagnostic testing methods

Introduction

Congenital heart disease (CHD) is one of the most common congenital malformations, and is a polygenic disease related to some major genes and involved in environmental factors. With the progress of science and technology, the progress was both in the studies of genetic patterns and testing methods. Understanding how each gene participates in normal and pathological anatomy is an important goal of CHD research. We reviewed the development of testing methods and CHD-related genes, to provide some enlightenment for the CHD prenatal diagnosis and hope to realize the intervention and treatment on the gene level of CHD in the future.

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来源期刊
Gynecology and Obstetrics Clinical Medicine
Gynecology and Obstetrics Clinical Medicine Medicine-Obstetrics and Gynecology
CiteScore
0.70
自引率
0.00%
发文量
35
审稿时长
18 weeks
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