A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly

Anomalous origin of coronary arteries is also a relatively rare congenital malformation and has been reported as the cause of angina pectoris and arrhythmia. Long QT syndrome (LQTS) is a rare inherited arrythmogenic disease characterized by susceptibility to life-threatening arrhytmias andsudden car...

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Autores principales: Karacaglar, Emir, Aydinalp, Alp, Coskun, Mehmet, Muderrisoglu, Haldun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981440/
https://www.ncbi.nlm.nih.gov/pubmed/24765385
http://dx.doi.org/10.4081/cp.2011.e85
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author Karacaglar, Emir
Aydinalp, Alp
Coskun, Mehmet
Muderrisoglu, Haldun
author_facet Karacaglar, Emir
Aydinalp, Alp
Coskun, Mehmet
Muderrisoglu, Haldun
author_sort Karacaglar, Emir
collection PubMed
description Anomalous origin of coronary arteries is also a relatively rare congenital malformation and has been reported as the cause of angina pectoris and arrhythmia. Long QT syndrome (LQTS) is a rare inherited arrythmogenic disease characterized by susceptibility to life-threatening arrhytmias andsudden cardiac death. We present a 36-year-old patient in whom two rare anomalies coexist and treated succesfully with β-blocker therapy.
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spelling pubmed-39814402014-04-24 A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly Karacaglar, Emir Aydinalp, Alp Coskun, Mehmet Muderrisoglu, Haldun Clin Pract Case Report Anomalous origin of coronary arteries is also a relatively rare congenital malformation and has been reported as the cause of angina pectoris and arrhythmia. Long QT syndrome (LQTS) is a rare inherited arrythmogenic disease characterized by susceptibility to life-threatening arrhytmias andsudden cardiac death. We present a 36-year-old patient in whom two rare anomalies coexist and treated succesfully with β-blocker therapy. PAGEPress Publications 2011-12-05 /pmc/articles/PMC3981440/ /pubmed/24765385 http://dx.doi.org/10.4081/cp.2011.e85 Text en ©Copyright E. Karacaglar et al., 2011 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy
spellingShingle Case Report
Karacaglar, Emir
Aydinalp, Alp
Coskun, Mehmet
Muderrisoglu, Haldun
A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly
title A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly
title_full A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly
title_fullStr A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly
title_full_unstemmed A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly
title_short A fatal combination in a young lady: Long QT syndrome and coronary artery anomaly
title_sort fatal combination in a young lady: long qt syndrome and coronary artery anomaly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981440/
https://www.ncbi.nlm.nih.gov/pubmed/24765385
http://dx.doi.org/10.4081/cp.2011.e85
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