Literature DB >> 28405885

Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications.

Cristian D'Ovidio1, Aldo Carnevale1, Vincenzo M Grassi2, Enrica Rosato1, Bernat Del Olmo3, Monica Coll3, Oscar Campuzano3, Anna Iglesias3, Ramon Brugada3, Antonio Oliva4.   

Abstract

This paper discusses the case of a young boy who died suddenly during a football match. The victim's personal and family medical histories were negative for cardiac events. He had undergone a cardiological investigation some months before his death, enabling him to participate in competitive sports. Only post-mortem molecular analysis allowed for a clearer determination of the most plausible cause of death, which was identified as inherited arrhythmogenic heart disease, known as catecholaminergic polymorphic ventricular tachycardia. It was possible to detect a novel, previously undescribed, variant in the RYR2 gene. This case report highlights the importance of a meaningful forensic multidisciplinary investigation in such cases, and also discusses possible medical malpractice claims.

Entities:  

Keywords:  Catecholaminergic polymorphic ventricular tachycardia; Provocation test; Rare variant; Stress electrocardiogram; Sudden cardiac death

Mesh:

Substances:

Year:  2017        PMID: 28405885     DOI: 10.1007/s12024-017-9862-9

Source DB:  PubMed          Journal:  Forensic Sci Med Pathol        ISSN: 1547-769X            Impact factor:   2.007


  52 in total

1.  Genetic analysis of sudden cardiac death victims: a survey of current forensic autopsy practices.

Authors:  Katarzyna Michaud; Patrice Mangin; Bernice S Elger
Journal:  Int J Legal Med       Date:  2010-06-11       Impact factor: 2.686

2.  When information can save lives: the duty to warn relatives about sudden cardiac death and environmental risks.

Authors:  Bernice Elger; Katarzyna Michaud; Patrice Mangin
Journal:  Hastings Cent Rep       Date:  2010 May-Jun       Impact factor: 2.683

3.  Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.

Authors:  A V Postma; I Denjoy; J Kamblock; M Alders; J-M Lupoglazoff; G Vaksmann; L Dubosq-Bidot; P Sebillon; M M A M Mannens; P Guicheney; A A M Wilde
Journal:  J Med Genet       Date:  2005-11       Impact factor: 6.318

4.  Sports-related sudden cardiac death in Switzerland classified by static and dynamic components of exercise.

Authors:  Christoph Gräni; Nina Chappex; Tony Fracasso; Cristina Vital; Christoph Kellerhals; Christian Schmied; Ardan M Saguner; Lukas D Trachsel; Prisca Eser; Katarzyna Michaud; Matthias Wilhelm
Journal:  Eur J Prev Cardiol       Date:  2016-02-25       Impact factor: 7.804

5.  Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

Authors:  Hanno L Tan; Nynke Hofman; Irene M van Langen; Allard C van der Wal; Arthur A M Wilde
Journal:  Circulation       Date:  2005-07-05       Impact factor: 29.690

Review 6.  Guidelines for the diagnosis and management of Catecholaminergic Polymorphic Ventricular Tachycardia.

Authors:  Andreas Pflaumer; Andrew M Davis
Journal:  Heart Lung Circ       Date:  2011-11-25       Impact factor: 2.975

Review 7.  State of postmortem genetic testing known as the cardiac channel molecular autopsy in the forensic evaluation of unexplained sudden cardiac death in the young.

Authors:  Michael J Ackerman
Journal:  Pacing Clin Electrophysiol       Date:  2009-07       Impact factor: 1.976

8.  Sudden cardiac death in the young (5-39 years) in the canton of Vaud, Switzerland.

Authors:  Fanny Hofer; Florence Fellmann; Jürg Schläpfer; Katarzyna Michaud
Journal:  BMC Cardiovasc Disord       Date:  2014-10-07       Impact factor: 2.298

9.  Ensembl 2016.

Authors:  Andrew Yates; Wasiu Akanni; M Ridwan Amode; Daniel Barrell; Konstantinos Billis; Denise Carvalho-Silva; Carla Cummins; Peter Clapham; Stephen Fitzgerald; Laurent Gil; Carlos García Girón; Leo Gordon; Thibaut Hourlier; Sarah E Hunt; Sophie H Janacek; Nathan Johnson; Thomas Juettemann; Stephen Keenan; Ilias Lavidas; Fergal J Martin; Thomas Maurel; William McLaren; Daniel N Murphy; Rishi Nag; Michael Nuhn; Anne Parker; Mateus Patricio; Miguel Pignatelli; Matthew Rahtz; Harpreet Singh Riat; Daniel Sheppard; Kieron Taylor; Anja Thormann; Alessandro Vullo; Steven P Wilder; Amonida Zadissa; Ewan Birney; Jennifer Harrow; Matthieu Muffato; Emily Perry; Magali Ruffier; Giulietta Spudich; Stephen J Trevanion; Fiona Cunningham; Bronwen L Aken; Daniel R Zerbino; Paul Flicek
Journal:  Nucleic Acids Res       Date:  2015-12-19       Impact factor: 16.971

10.  An integrated map of genetic variation from 1,092 human genomes.

Authors:  Goncalo R Abecasis; Adam Auton; Lisa D Brooks; Mark A DePristo; Richard M Durbin; Robert E Handsaker; Hyun Min Kang; Gabor T Marth; Gil A McVean
Journal:  Nature       Date:  2012-11-01       Impact factor: 49.962

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.