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Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations
Genetic channelopathies can predispose individuals to life-threatening arrhythmias. Two such channelopathies are long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT). To the best of our knowledge, we present the first case of LQTS with novel combined genetic mutat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636151/ https://www.ncbi.nlm.nih.gov/pubmed/34873534 http://dx.doi.org/10.7759/cureus.19195 |
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author | Lakhana, Muhddesa McGee, James George, Blessen Whang, William Kanner, Lawrence Park, Won Jun |
author_facet | Lakhana, Muhddesa McGee, James George, Blessen Whang, William Kanner, Lawrence Park, Won Jun |
author_sort | Lakhana, Muhddesa |
collection | PubMed |
description | Genetic channelopathies can predispose individuals to life-threatening arrhythmias. Two such channelopathies are long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT). To the best of our knowledge, we present the first case of LQTS with novel combined genetic mutations of KCNH2 and cardiac ryanodine receptor (RYR2) genes. |
format | Online Article Text |
id | pubmed-8636151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-86361512021-12-05 Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations Lakhana, Muhddesa McGee, James George, Blessen Whang, William Kanner, Lawrence Park, Won Jun Cureus Cardiology Genetic channelopathies can predispose individuals to life-threatening arrhythmias. Two such channelopathies are long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT). To the best of our knowledge, we present the first case of LQTS with novel combined genetic mutations of KCNH2 and cardiac ryanodine receptor (RYR2) genes. Cureus 2021-11-01 /pmc/articles/PMC8636151/ /pubmed/34873534 http://dx.doi.org/10.7759/cureus.19195 Text en Copyright © 2021, Lakhana et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Cardiology Lakhana, Muhddesa McGee, James George, Blessen Whang, William Kanner, Lawrence Park, Won Jun Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations |
title | Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations |
title_full | Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations |
title_fullStr | Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations |
title_full_unstemmed | Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations |
title_short | Simultaneous Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Gene Mutations |
title_sort | simultaneous catecholaminergic polymorphic ventricular tachycardia and long qt syndrome gene mutations |
topic | Cardiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636151/ https://www.ncbi.nlm.nih.gov/pubmed/34873534 http://dx.doi.org/10.7759/cureus.19195 |
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