Felix Janine F, de Jong Elisabeth M, Torfs Claudine P, de Klein A, Rottier Robbert J, Tibboel Dick
Department of Pediatric Surgery, Erasmus MC-Sophia Children's Hospital, 3000 CB Rotterdam, the Netherlands.
Birth Defects Res A Clin Mol Teratol. 2009 Sep;85(9):747-54. doi: 10.1002/bdra.20592.
Esophageal atresia and/or tracheoesophageal fistula (EA/TEF) are severe congenital anomalies. Although recent years have brought significant improvement in clinical treatment, our understanding of the etiology of these defects is lagging. Many genes and genetic pathways have been implicated in the development of EA/TEF, but only a few genes have been shown to be involved in humans, in animals, or in both. Extrapolating data from animal models to humans is not always straightforward. Environmental factors may also carry a risk, but the mechanisms are yet to be elucidated. This review gives an overview of the current state of knowledge about both genetic and environmental risk factors in the etiology of EA/TEF.
食管闭锁和/或气管食管瘘(EA/TEF)是严重的先天性畸形。尽管近年来临床治疗有了显著改善,但我们对这些缺陷病因的了解仍很滞后。许多基因和遗传通路与EA/TEF的发生有关,但只有少数基因在人类、动物或两者中均被证实与之相关。将动物模型的数据外推至人类并非总是简单直接的。环境因素也可能带来风险,但其机制尚待阐明。本综述概述了目前关于EA/TEF病因中遗传和环境风险因素的知识现状。