https://pediatrics.medresearch.in/index.php/ijpr/issue/feed Pediatric Review: International Journal of Pediatric Research 2021-04-20T19:39:31+0530 Dr D Sharad Gedam editor@pediatrics.medresearch.in Open Journal Systems <p><em><strong>ISSN: <a href="https://portal.issn.org/resource/ISSN/2349-3267" target="_blank" rel="noopener">2349-3267 (Online)</a>, <a href="https://portal.issn.org/resource/ISSN/2349-5499" target="_blank" rel="noopener">2349-5499 (Print)</a></strong></em></p> https://pediatrics.medresearch.in/index.php/ijpr/article/view/663 Tracheal agenesis: a rare congenital disorder 2021-04-20T19:39:31+0530 Dr. Ravali Gundapuneni Rao ravaliraog@gmail.com Dr. Balaji Susarla Venkata Rama susbalaji3@gmail.com Dr. Harshitha Gattu gattu.harshi@gmail.com Dr. Alekya Paripati alekhyareddy1@yahoo.com <p>Tracheal agenesis is a severe congenital disorder with often an emergency presentation. There is a complete or partial absence of the trachea below the larynx, with the presence or absence of a tracheoesophageal fistula. It is a rare differential diagnosis of postnatal respiratory distress and the obstetrician or neonatologist will regularly be surprised by this malformation. The etiology of Tracheal atresia is unknown, therapeutic options are limited thus making this condition a usually fatal disorder. In most cases, congenital anomalies of the heart, digestive tract or GUT are present. The main signs are respiratory distress and cyanosis, inability to vocalize and impossible tracheal intubation. Isolated tracheal agenesis without any malformation is very rare. Here we report a case of a preterm neonate born at 33 weeks gestation with tracheal agenesis with no other associated malformation. In most cases, the seldom deformation, tracheal agenesis does not get recognized before the child is born.</p> 2021-04-20T00:00:00+0530 Copyright (c) 2021 Author (s). Published by Siddharth Health Research and Social Welfare Society