Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-dfsvx Total loading time: 0 Render date: 2024-04-26T20:12:01.893Z Has data issue: false hasContentIssue false

Chapter 29 - Cardiac Arrhythmias

from Section 7 - Pathophysiology

Published online by Cambridge University Press:  04 June 2019

Marta C. Cohen
Affiliation:
Sheffield Children’s Hospital
Irene B. Scheimberg
Affiliation:
Royal London Hospital
J. Bruce Beckwith
Affiliation:
Loma Linda University School of Medicine
Fern R. Hauck
Affiliation:
University of Virginia
Get access

Summary

Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2019

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Eilbeck, K, Quinlan, A, Yandell, M. Settling the score: variant prioritization and Mendelian disease. Nat Rev Genet, 2017; 18(10):599612.Google Scholar
McRae, JF, et al. Deciphering developmental disorder study. Prevalence and architecture of de novo mutations in developmental disorders. Nature, 2017; 542(7642):433–8.Google Scholar
Priori, SG, Wilde, AA, Horie, M, Cho, Y, Behr, ER, Berul, C, et al. HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. Heart Rhythm, 2013; 10(12):1932–63.Google Scholar
Priori, SG, Blomstrom-Lundqvist, C. European Society of Cardiology guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death summarized by co-chairs. Eur Heart J, 2015; 36(41):2757–9.Google Scholar
Ioakeimidis, NS, Papamitsou, T, Meditskou, S, Iakovidou-Kritsi, Z. Sudden Infant Death Syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence. J Biol Res (Thessalon), 2017; 24:6; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348737/ (accessed 31 October 2018).CrossRefGoogle Scholar
Schwartz, PJ, Moss, AJ, Vincent, GM, Crampton, RS. Diagnostic criteria for the long QT syndrome. An update. Circulation, 1993; 88(2):782.Google Scholar
Schwartz, PJ, Stramba-Badiale, M, Crotti, L, Pedrazzini, M, Besana, A, Bosi, G, et al. Prevalence of the congenital long QT Syndrome. Circulation, 2009; 120(18):1761–7.CrossRefGoogle ScholarPubMed
Maron, BJ, Clark, CE, Goldstein, RE, Epstein, SE. Potential role of QT interval prolongation in Sudden Infant Death Syndrome. Circulation, 1976; 54(3):423–30.Google Scholar
Schwartz, PJ, Stramba-Badiale, M, Segantini, A, Austoni, P, Bosi, G, Giorgetti, R, et al. Prolongation of the QT interval and the Sudden Infant Death Syndrome. N Engl J Med, 1998; 338(24):1709–14.Google Scholar
Mizusawa, Y, Horie, M Wilde, AM, Wilde, AA. Genetic and clinical advances in congenital long QT syndrome. Circ J, 2014; 78(12):2827–33.CrossRefGoogle ScholarPubMed
Weiss, JN, Garfinkel, A, Karagueuzian, HS, Chen, P, Qu, Z. Early afterdepolarizations and cardiac arrhythmias. Heart Rhythm, 2010; 7(12):1891–9.Google Scholar
Baruteau, A-E, Tester, DJ, Kapplinger, JD, Ackerman, MJ, Behr, ER. Sudden Infant Death Syndrome and inherited cardiac conditions. Nat Rev Cardiol, 2017; 14 (12):715–26.CrossRefGoogle ScholarPubMed
Tester, DJ, Ackerman, MJ. Sudden Infant Death Syndrome: how significant are the cardiac channelopathies? Cardiovasc Res, 2005; 67(3):388–96.CrossRefGoogle ScholarPubMed
Arnestad, M, Crotti, L, Rognum, TO, Insolia, RF, Pedrazzini, MF, Ferrandi, CF, et al. Prevalence of long-QT syndrome gene variants in Sudden Infant Death Syndrome. Circulation, 2007;115(3):361–7.Google Scholar
Kamakura, S. Epidemiology of Brugada syndrome in Japan and rest of the world. J Arrhythmia; Special Issue: Brugada Syndrome from Bench to Bedside, 2013; 29(2):52–5.Google Scholar
Kapplinger, JD, Tester, DJ, Alders, MF, Benito, BF, Berthet, MF, Brugada, JF, et al. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing. Heart Rhythm, 2010; 7(1):3346.Google Scholar
Remme, CA. Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular, and genetic aspects. J Physiol (Lond), 2013; 591:4099–116.Google Scholar
Priori, SG, Napolitano, C, Giordano, U, Collisani, G, Memmi, M. Brugada syndrome and sudden cardiac death in children. Lancet, 2000; 355(9206):808–9.Google Scholar
Tan, BH, Pundi, KN, Van Norstrand, DW, Valdivia, CR, Tester, DJ, Medeiros-Domingo, A, et al. Sudden Infant Death Syndrome-associated mutations in the sodium channel beta subunits. Heart Rhythm, 2010; 7(6):771–8.CrossRefGoogle ScholarPubMed
Landstrom, AP, Dobrev, D, Wehrens, XHT. Calcium signaling and cardiac arrhythmias. Circ Res, 2017; 120(12):1969.CrossRefGoogle ScholarPubMed
Tester, DJ, Dura, M, Carturan, E, Reiken, S, Wronska, A, Marks, AR, et al. A mechanism for Sudden Infant Death Syndrome (SIDS): stress-induced leak via ryanodine receptors. Heart Rhythm, 2007; 4(6):733–9.Google Scholar
Larsen, MK, Berge, KE, Leren, TP, Nissen, PH, Hansen, J, Kristensen, IB, et al. Postmortem genetic testing of the ryanodine receptor 2 (RYR2) gene in a cohort of sudden unexplained death cases. Int J Legal Med, 2013; 127(1):139–44.Google Scholar
Patel, C, Yan, G, Antzelevitch, C. Short QT syndrome: from bench to bedside. Circ Arrhythm Electrophysiol, 2010; 3(4):401–8.CrossRefGoogle ScholarPubMed
Miles, CJ, Behr, ER. The role of genetic testing in unexplained sudden death. Transl Res, 2016; 168:5973.CrossRefGoogle ScholarPubMed
Lahrouchi, N, Raju, H, Lodder, EM, Papatheodorou, E, Ware, JS, Papadakis, M, et al. Utility of post-mortem genetic testing in cases of Sudden Arrhythmic Death Syndrome. J Am Coll Cardiol, 2017; 69(17):2134–45.Google Scholar
Ackerman, MJ. Genetic purgatory and the cardiac channelopathies: exposing the variants of uncertain/unknown significance issue. Heart Rhythm, 2015; 12(11):2325–31.CrossRefGoogle ScholarPubMed
Neubauer, J, Lecca, MR, Russo, G, Bartsch, C, Medeiros-Domingo, A, Berger, W, et al. Post-mortem whole-exome analysis in a large Sudden Infant Death Syndrome cohort with a focus on cardiovascular and metabolic genetic diseases. Eur J Hum Gen, 2017; 25(4):404–9.Google Scholar
Plant, LD, Bowers, PN, Liu, Q, Morgan, T, Zhang, T, State, MW, et al. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. J Clin Invest, 2005; 116(2):430–5.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×