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Congenital long QT syndrome and patent ductus arteriosus: A rare surgical scenario
Congenital long QT syndrome (LQTS) is a rare cardiac condition characterized by abnormality of either sodium or potassium ion channels resulting in prolongation of QT interval and thereby predisposing to life-threatening arrhythmia. Once the syndrome is diagnosed, measures should be taken to avoid s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918017/ https://www.ncbi.nlm.nih.gov/pubmed/33679068 http://dx.doi.org/10.4103/apc.APC_146_19 |
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author | Raja, Javid Menon, Sabarinath Venkata, Devarakonda Bhargava Unnikrishnan, KP Namboodiri, Narayanan |
author_facet | Raja, Javid Menon, Sabarinath Venkata, Devarakonda Bhargava Unnikrishnan, KP Namboodiri, Narayanan |
author_sort | Raja, Javid |
collection | PubMed |
description | Congenital long QT syndrome (LQTS) is a rare cardiac condition characterized by abnormality of either sodium or potassium ion channels resulting in prolongation of QT interval and thereby predisposing to life-threatening arrhythmia. Once the syndrome is diagnosed, measures should be taken to avoid sudden cardiac death. We present a rare case of LQTS associated with patent ductus arteriosus in a child, and a unique approach was used in managing both conditions. |
format | Online Article Text |
id | pubmed-7918017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-79180172021-03-05 Congenital long QT syndrome and patent ductus arteriosus: A rare surgical scenario Raja, Javid Menon, Sabarinath Venkata, Devarakonda Bhargava Unnikrishnan, KP Namboodiri, Narayanan Ann Pediatr Cardiol Case Report Congenital long QT syndrome (LQTS) is a rare cardiac condition characterized by abnormality of either sodium or potassium ion channels resulting in prolongation of QT interval and thereby predisposing to life-threatening arrhythmia. Once the syndrome is diagnosed, measures should be taken to avoid sudden cardiac death. We present a rare case of LQTS associated with patent ductus arteriosus in a child, and a unique approach was used in managing both conditions. Wolters Kluwer - Medknow 2021 2020-09-23 /pmc/articles/PMC7918017/ /pubmed/33679068 http://dx.doi.org/10.4103/apc.APC_146_19 Text en Copyright: © 2020 Annals of Pediatric Cardiology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Raja, Javid Menon, Sabarinath Venkata, Devarakonda Bhargava Unnikrishnan, KP Namboodiri, Narayanan Congenital long QT syndrome and patent ductus arteriosus: A rare surgical scenario |
title | Congenital long QT syndrome and patent ductus arteriosus: A rare surgical scenario |
title_full | Congenital long QT syndrome and patent ductus arteriosus: A rare surgical scenario |
title_fullStr | Congenital long QT syndrome and patent ductus arteriosus: A rare surgical scenario |
title_full_unstemmed | Congenital long QT syndrome and patent ductus arteriosus: A rare surgical scenario |
title_short | Congenital long QT syndrome and patent ductus arteriosus: A rare surgical scenario |
title_sort | congenital long qt syndrome and patent ductus arteriosus: a rare surgical scenario |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918017/ https://www.ncbi.nlm.nih.gov/pubmed/33679068 http://dx.doi.org/10.4103/apc.APC_146_19 |
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