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Down syndrome child with multiple heart diseases: A case report

BACKGROUND: Down syndrome, also known as trisomy 21 syndrome, is commonly associated with congenital heart disease, and can often result in early formation of pulmonary hypertension. The development of pulmonary hypertension can result from factors such as intracardiac and macrovascular shunts, and...

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Autores principales: Kong, Mo-Wei, Li, Yi-Jing, Li, Jun, Pei, Zhen-Ying, Xie, Yu-Yu, He, Guo-Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696207/
http://dx.doi.org/10.4330/wjc.v15.i11.615
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author Kong, Mo-Wei
Li, Yi-Jing
Li, Jun
Pei, Zhen-Ying
Xie, Yu-Yu
He, Guo-Xiang
author_facet Kong, Mo-Wei
Li, Yi-Jing
Li, Jun
Pei, Zhen-Ying
Xie, Yu-Yu
He, Guo-Xiang
author_sort Kong, Mo-Wei
collection PubMed
description BACKGROUND: Down syndrome, also known as trisomy 21 syndrome, is commonly associated with congenital heart disease, and can often result in early formation of pulmonary hypertension. The development of pulmonary hypertension can result from factors such as intracardiac and macrovascular shunts, and upper airway obstruction or hypoplasia of lung tissue. Individuals with Down syndrome and congenital heart disease have a significantly lower average life expectancy, with surgical intervention being the most viable treatment option to improve longevity. CASE SUMMARY: We report the case of a 13-year-old boy with Down syndrome presenting with atrial septal defect and patent ductus arteriosus along with severe pulmonary hypertension. The electrocardiogram shows sinus rhythm and right ventricular hypertrophy. The echocardiogram shows an atrial septal defect with interrupted echo in the interatrial septum, measuring 0.813 cm in length. The patient was initially refused to be offered surgical treatment by many hospitals due to the high surgical risk and pulmonary artery resistance. After discussing the patient’s diagnosis and treatment options, we ultimately recommended surgical treatment. However, the patient and their family declined this recommendation and chose to be discharged. During the follow-up period of 6 mo, there were no significant improvements or deteriorations in the patient’s condition. CONCLUSION: In conclusion, this case highlights the challenges faced by individuals with Down syndrome and congenital heart disease complicated by severe pulmonary hypertension. Timely intervention and a multidisciplinary approach are crucial for improving prognosis and life expectancy. Further research is needed to enhance our understanding and develop effective interventions for this population.
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spelling pubmed-106962072023-12-06 Down syndrome child with multiple heart diseases: A case report Kong, Mo-Wei Li, Yi-Jing Li, Jun Pei, Zhen-Ying Xie, Yu-Yu He, Guo-Xiang World J Cardiol Case Report BACKGROUND: Down syndrome, also known as trisomy 21 syndrome, is commonly associated with congenital heart disease, and can often result in early formation of pulmonary hypertension. The development of pulmonary hypertension can result from factors such as intracardiac and macrovascular shunts, and upper airway obstruction or hypoplasia of lung tissue. Individuals with Down syndrome and congenital heart disease have a significantly lower average life expectancy, with surgical intervention being the most viable treatment option to improve longevity. CASE SUMMARY: We report the case of a 13-year-old boy with Down syndrome presenting with atrial septal defect and patent ductus arteriosus along with severe pulmonary hypertension. The electrocardiogram shows sinus rhythm and right ventricular hypertrophy. The echocardiogram shows an atrial septal defect with interrupted echo in the interatrial septum, measuring 0.813 cm in length. The patient was initially refused to be offered surgical treatment by many hospitals due to the high surgical risk and pulmonary artery resistance. After discussing the patient’s diagnosis and treatment options, we ultimately recommended surgical treatment. However, the patient and their family declined this recommendation and chose to be discharged. During the follow-up period of 6 mo, there were no significant improvements or deteriorations in the patient’s condition. CONCLUSION: In conclusion, this case highlights the challenges faced by individuals with Down syndrome and congenital heart disease complicated by severe pulmonary hypertension. Timely intervention and a multidisciplinary approach are crucial for improving prognosis and life expectancy. Further research is needed to enhance our understanding and develop effective interventions for this population. Baishideng Publishing Group Inc 2023-11-26 2023-11-26 /pmc/articles/PMC10696207/ http://dx.doi.org/10.4330/wjc.v15.i11.615 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Case Report
Kong, Mo-Wei
Li, Yi-Jing
Li, Jun
Pei, Zhen-Ying
Xie, Yu-Yu
He, Guo-Xiang
Down syndrome child with multiple heart diseases: A case report
title Down syndrome child with multiple heart diseases: A case report
title_full Down syndrome child with multiple heart diseases: A case report
title_fullStr Down syndrome child with multiple heart diseases: A case report
title_full_unstemmed Down syndrome child with multiple heart diseases: A case report
title_short Down syndrome child with multiple heart diseases: A case report
title_sort down syndrome child with multiple heart diseases: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696207/
http://dx.doi.org/10.4330/wjc.v15.i11.615
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