Felix J F, Keijzer R, van Dooren M F, Rottier R J, Tibboel D
Department of Paediatric Surgery, Erasmus MC--Sophia Children's Hospital, Rotterdam, The Netherlands.
Pediatr Surg Int. 2004 Oct;20(10):731-6. doi: 10.1007/s00383-004-1287-3.
Oesophageal atresia and tracheo-oesophageal fistula are relatively frequently occurring foregut malformations of which the aetiology and pathogenesis are poorly understood. Recent results of molecular genetic studies, in particular the use of single and compound mutant mice, have yielded a tremendous increase in the understanding of the molecular mechanisms involved in normal and abnormal foregut morphogenesis. In the introduction of this paper, we review the very early stages of normal and abnormal embryology of the foregut derivatives and the separation of the foregut into a ventral respiratory part and a dorsal digestive part. After that, we describe the genes that have been demonstrated to play an important role in these processes.
食管闭锁和气管食管瘘是相对常见的前肠畸形,其病因和发病机制尚不清楚。分子遗传学研究的最新结果,特别是单突变和复合突变小鼠的应用,极大地增进了我们对正常和异常前肠形态发生所涉及分子机制的理解。在本文引言中,我们回顾了前肠衍生物正常和异常胚胎发育的早期阶段,以及前肠分为腹侧呼吸部分和背侧消化部分的过程。之后,我们描述了已证实在这些过程中起重要作用的基因。