| Literature DB >> 29754141 |
Sudheer R Gorla1, Josaura Fernandez-Sanchez1, Ashish Garg1, Sethuraman Swaminathan1.
Abstract
Unilateral lung agenesis is a relatively rare congenital anomaly with a reported incidence of 1 in 15 000 births. It is frequently associated with other congenital malformations. Some of the sequelae of lung agenesis are potentially life-threatening. Here, we report a case of left lung agenesis in association with hiatal hernia and atrioventricular septal defect, a rare combination of anomalies which have not been described previously in the literature. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: congenital disorders; neonatal intensive care; pulmonary hypertension; stomach and duodenum
Mesh:
Year: 2018 PMID: 29754141 PMCID: PMC6040498 DOI: 10.1136/bcr-2018-224382
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X