Emanuel R
Br Heart J. 1970 May;32(3):281-91. doi: 10.1136/hrt.32.3.281.
In isolated congenital heart disease genetic factors have been shown from family studies, individual pedigree analyses, the frequency of consanguinity, examination of data from twins, and possibly from cytogenetics. In defects of the atrial septum, where data are most complete, genetic factors appear to be important, particularly in secundum atrial septal defect. In the syndromes with abnormal chromosomes in which congenital heart disease is common, the cardiovascular abnormality is probably directly associated with the abnormal genetic material present. In hereditary disorders with normal chromosomes in which congenital heart disease features, the pattern of inheritance suggests transmission by a single gene or group of genes. The cardiovascular abnormality is genetically determined, though it may not become apparent until many years after birth.
在孤立性先天性心脏病中,通过家族研究、个体系谱分析、近亲结婚频率、双胞胎数据研究以及可能的细胞遗传学研究,已证实存在遗传因素。在房间隔缺损方面,相关数据最为完整,遗传因素似乎起着重要作用,尤其是继发孔型房间隔缺损。在先天性心脏病常见的染色体异常综合征中,心血管异常可能与所存在的异常遗传物质直接相关。在染色体正常但伴有先天性心脏病特征的遗传性疾病中,遗传模式表明由单个基因或一组基因传递。心血管异常是由遗传决定的,尽管可能在出生多年后才会显现出来。