A Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations

A 3-year-old Chinese boy was diagnosed with ipsilateral congenital malformations: right lung hypoplasia, dextroversion of heart, atrial septal defect, hepatic vein drainage directly into the right atrium, facial asymmetry, right microtia and congenital deafness, and indirect inguinal hernia. He unde...

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Detalles Bibliográficos
Autores principales: Fan, Chengming, Huang, Can, Liu, Jijia, Yang, Jinfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532940/
https://www.ncbi.nlm.nih.gov/pubmed/26294998
http://dx.doi.org/10.1155/2015/741540
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author Fan, Chengming
Huang, Can
Liu, Jijia
Yang, Jinfu
author_facet Fan, Chengming
Huang, Can
Liu, Jijia
Yang, Jinfu
author_sort Fan, Chengming
collection PubMed
description A 3-year-old Chinese boy was diagnosed with ipsilateral congenital malformations: right lung hypoplasia, dextroversion of heart, atrial septal defect, hepatic vein drainage directly into the right atrium, facial asymmetry, right microtia and congenital deafness, and indirect inguinal hernia. He underwent indirect inguinal hernia repair at the age of 2. Although without any facial plastic surgery performed, he underwent a repair of atrial septal defect and recovered uneventfully. At 6-month follow-up, the patient was free from any symptom of dyspnea; his heart function returned to the first grade.
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spelling pubmed-45329402015-08-20 A Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations Fan, Chengming Huang, Can Liu, Jijia Yang, Jinfu Case Rep Pediatr Case Report A 3-year-old Chinese boy was diagnosed with ipsilateral congenital malformations: right lung hypoplasia, dextroversion of heart, atrial septal defect, hepatic vein drainage directly into the right atrium, facial asymmetry, right microtia and congenital deafness, and indirect inguinal hernia. He underwent indirect inguinal hernia repair at the age of 2. Although without any facial plastic surgery performed, he underwent a repair of atrial septal defect and recovered uneventfully. At 6-month follow-up, the patient was free from any symptom of dyspnea; his heart function returned to the first grade. Hindawi Publishing Corporation 2015 2015-07-29 /pmc/articles/PMC4532940/ /pubmed/26294998 http://dx.doi.org/10.1155/2015/741540 Text en Copyright © 2015 Chengming Fan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Fan, Chengming
Huang, Can
Liu, Jijia
Yang, Jinfu
A Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations
title A Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations
title_full A Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations
title_fullStr A Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations
title_full_unstemmed A Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations
title_short A Child with Lung Hypoplasia, Congenital Heart Disease, Hemifacial Microsomia, and Inguinal Hernia: Ipsilateral Congenital Malformations
title_sort child with lung hypoplasia, congenital heart disease, hemifacial microsomia, and inguinal hernia: ipsilateral congenital malformations
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532940/
https://www.ncbi.nlm.nih.gov/pubmed/26294998
http://dx.doi.org/10.1155/2015/741540
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