Schüler L, Salzano F M
Unidade de Genética Médica, Hospital de Clínicas de Porto Alegre RS, Brazil.
Am J Med Genet. 1994 Jan 1;49(1):29-35. doi: 10.1002/ajmg.1320490108.
Starting from a data base of over one million births investigated in 11 countries as a part of the Latin American Study of Congenital Malformations, 1,428 babies with three or more malformations without known pathogenesis or cause were studied. The objective was to search for statistically significant associations between defects and the delineation of new syndromes. One hundred and twenty-one patients presented an association between malformations of the digestive and urogenital systems involving mainly anal, renal, and genital anomalies, while 21 of them had 3 or more VACTERL defects. The frequencies of these defects were intermediate between those observed for VACTERL or sirenomelia, supporting the idea that these conditions have a similar pathogenesis. Statistical approaches like this one may be helpful in identifying processes and biological entities that may be missed using simple clinical observations.
作为拉丁美洲先天性畸形研究的一部分,从11个国家调查的超过100万例出生数据中,对1428名有三种或更多畸形且病因不明的婴儿进行了研究。目的是寻找缺陷之间具有统计学意义的关联,并确定新的综合征。121名患者的消化和泌尿生殖系统畸形之间存在关联,主要涉及肛门、肾脏和生殖器异常,其中21名患者有3种或更多VACTERL缺陷。这些缺陷的频率介于VACTERL或并腿畸形所观察到的频率之间,支持了这些病症具有相似发病机制的观点。这样的统计方法可能有助于识别使用简单临床观察可能遗漏的过程和生物实体。