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A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus

Laryngeal atresia is generally a fatal congenital anomaly with an incidence of 1: 50,000 births. This congenital anomaly is a condition of multifactorial inheritance, in which the fetus has a dilated trachea, enlarged echogenic lungs, an inverted or flattened diaphragm, fetal hydrops, and ascites. D...

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Autores principales: Korkmaz, Levent, Güneş, Işın, Halis, Hülya, Ketenci, İbrahim, Baştuğ, Osman, Doğan, Mehmet Said, Akın, Mustafa Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559978/
https://www.ncbi.nlm.nih.gov/pubmed/31217712
http://dx.doi.org/10.5152/TurkPediatriArs.2018.4619
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author Korkmaz, Levent
Güneş, Işın
Halis, Hülya
Ketenci, İbrahim
Baştuğ, Osman
Doğan, Mehmet Said
Akın, Mustafa Ali
author_facet Korkmaz, Levent
Güneş, Işın
Halis, Hülya
Ketenci, İbrahim
Baştuğ, Osman
Doğan, Mehmet Said
Akın, Mustafa Ali
author_sort Korkmaz, Levent
collection PubMed
description Laryngeal atresia is generally a fatal congenital anomaly with an incidence of 1: 50,000 births. This congenital anomaly is a condition of multifactorial inheritance, in which the fetus has a dilated trachea, enlarged echogenic lungs, an inverted or flattened diaphragm, fetal hydrops, and ascites. Diagnosis is usually made when there is failure to perform endotracheal intubation in a neonate with severe respiratory distress and absence of audible cry. Here, we present a very rare case of a newborn with laryngeal atresia who had respiratory distress and was sustained for the first few minutes of life using partial ventilation via a persistent pharyngotracheal duct. We would like to draw the attention of all physicians to this issue by reporting a rare fatal case of a newborn with a congenital presentation.
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spelling pubmed-65599782019-06-19 A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus Korkmaz, Levent Güneş, Işın Halis, Hülya Ketenci, İbrahim Baştuğ, Osman Doğan, Mehmet Said Akın, Mustafa Ali Turk Pediatri Ars Case Report Laryngeal atresia is generally a fatal congenital anomaly with an incidence of 1: 50,000 births. This congenital anomaly is a condition of multifactorial inheritance, in which the fetus has a dilated trachea, enlarged echogenic lungs, an inverted or flattened diaphragm, fetal hydrops, and ascites. Diagnosis is usually made when there is failure to perform endotracheal intubation in a neonate with severe respiratory distress and absence of audible cry. Here, we present a very rare case of a newborn with laryngeal atresia who had respiratory distress and was sustained for the first few minutes of life using partial ventilation via a persistent pharyngotracheal duct. We would like to draw the attention of all physicians to this issue by reporting a rare fatal case of a newborn with a congenital presentation. Kare Publishing 2019-03-01 /pmc/articles/PMC6559978/ /pubmed/31217712 http://dx.doi.org/10.5152/TurkPediatriArs.2018.4619 Text en Copyright: © 2019 Turkish Pediatric Association http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Case Report
Korkmaz, Levent
Güneş, Işın
Halis, Hülya
Ketenci, İbrahim
Baştuğ, Osman
Doğan, Mehmet Said
Akın, Mustafa Ali
A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus
title A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus
title_full A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus
title_fullStr A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus
title_full_unstemmed A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus
title_short A case of laryngeal atresia accompanied by persistent pharyngotracheal ductus
title_sort case of laryngeal atresia accompanied by persistent pharyngotracheal ductus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559978/
https://www.ncbi.nlm.nih.gov/pubmed/31217712
http://dx.doi.org/10.5152/TurkPediatriArs.2018.4619
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