Synchronous cardiac arrest in monozygotic twins with hypertrophic cardiomyopathy - Is sudden cardiac death genetically pre-programmed?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/article/10.1186/s12872-015-0007-3/fulltext.html
Reference9 articles.
1. Alcalai R, Seidman JG, Seidman CE. Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics. J Cardiovasc Electrophysiol. 2008;19(1):104–10.
2. Maron BJ, Seidman CE, Ackerman MJ, Towbin JA, Maron MS, Ommen SR, et al. How should hypertrophic cardiomyopathy be classified?: What’s in a name? Dilemmas in nomenclature characterizing hypertrophic cardiomyopathy and left ventricular hypertrophy. Circ Cardiovasc Genet. 2009;2(1):81–5. discussion 6.
3. Puranik R, Chow CK, Duflou JA, Kilborn MJ, McGuire MA. Sudden death in the young. Heart Rhythm. 2005;2(12):1277–82.
4. Adabag AS, Maron BJ. Implications of arrhythmias and prevention of sudden death in hypertrophic cardiomyopathy. Ann Noninvasive Electrocardiol. 2007;12(2):171–80.
5. Maron BJ, Casey SA, Almquist AK. Images in cardiovascular medicine. Hypertrophic cardiomyopathy in monozygotic twins. Circulation. 2002;105(18):2229.
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1. Hypertrophic cardiomyopathy in identical twins: a case series;European Heart Journal - Case Reports;2022-11-28
2. Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy;Life;2022-08-30
3. Adult Monozygotic Twins With Hypertrophic Cardiomyopathy and Identical Disease Expression and Clinical Course;The American Journal of Cardiology;2020-07
4. Different Clinical Presentation and Tissue Characterization in a Monozygotic Twin Pair with MYH7 Mutation-Related Hypertrophic Cardiomyopathy;International Heart Journal;2019-03-30
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