Infantile hypertrophic pyloric stenosis in patients with esophageal atresia.
Chantal A Ten KateRutger W W BrouwerYolande van BeverVera K MartensTom BrandsNicole W G van BeelenAlice S BrooksDaphne HuighRobert M van der HelmBert H F M M EussenWilfred F J van IJckenHanneke IJsselstijnDick TibboelRene M H WijnenAnnelies de KleinRobert M W HofstraErwin BrosensPublished in: Birth defects research (2020)
None of our findings could fully explain the combination of abnormalities on its own, which makes complex inheritance the most plausible genetic explanation, most likely in combination with mechanical and/or environmental factors. As we did not find one defining monogenetic cause for the EA/IHPS phenotype, the impact of the corrective surgery could should be further investigated.