Czeizel A, Ludányi I
Eur J Pediatr. 1985 Nov;144(4):331-7. doi: 10.1007/BF00441773.
This paper reports the results of the first population-based study of the aetiology of VACTERL-association (i.e., the occurrence of three or more closely defined VACTERL-type abnormalities without other major congenital abnormalities). Forty-three VACTERL-associations and 33 VACTERL-like cases (the latter representing combinations of three or more closely or broadly defined VACTERL abnormalities with other congenital abnormalities) were evaluated. The noteworthy features of the VACTERL-association are: a significant male preponderance, a fetal weight retardation in full-term pregnancies, planned conceptions occurring later than in general and a higher incidence of infertility problems. Our data support the thesis that genetic factors are probably not involved in the aetiology of the VACTERL-association. In contrast, the VACTERL-like cases have a female excess, a higher rate of advanced birth order, no disturbance in fertility and some specific familial occurrence. These findings strongly suggest that genetic factors play a role in the aetiology of this heterogeneous group of multiple congenital abnormalities.
本文报告了第一项基于人群的VACTERL综合征病因研究结果(即出现三种或更多紧密定义的VACTERL型异常且无其他主要先天性异常)。对43例VACTERL综合征和33例VACTERL样病例(后者代表三种或更多紧密或宽泛定义的VACTERL异常与其他先天性异常的组合)进行了评估。VACTERL综合征的显著特征为:男性明显居多、足月妊娠时胎儿体重发育迟缓、计划受孕时间晚于一般情况以及不孕问题发生率较高。我们的数据支持遗传因素可能不参与VACTERL综合征病因的论点。相比之下,VACTERL样病例女性居多、高龄产次比例较高、生育无紊乱且有一些特定的家族性发病情况。这些发现强烈表明遗传因素在这一异质性多重先天性异常组的病因中起作用。