Arrhythmogenic Right Ventricular Cardiomyopathy in a Pediatric Patient Case Report: Clinical Case

Rob Roudijk; R. Evertz; Arco Teske; C. Marcelis; Dennis G H Bosboom; BK Velthuis; F.E.A. Udink ten Cate; Anneline S.J.M. te Riele

doi:10.1016/j.jaccas.2020.01.006

Arrhythmogenic Right Ventricular Cardiomyopathy in a Pediatric Patient Case Report: Clinical Case

Rob Roudijk
, R. Evertz
, Arco Teske
, C. Marcelis
, Dennis G H Bosboom
, BK Velthuis
, F.E.A. Udink ten Cate
, Anneline S.J.M. te Riele

Research output: Contribution to journal › Article › Academic › peer-review

17 Downloads (Pure)

Abstract

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is rarely diagnosed in childhood. We describe the case of a 9-year-old girl with genetically confirmed ARVC who presented with syncope, ventricular arrhythmia, and biventricular myocardial dysfunction. This case highlights the need for development of pediatric ARVC diagnosis criteria specific for pediatric patients and discusses potential diagnostic improvement using echocardiographic deformation imaging. (Level of Difficulty: Beginner.)

Original language	English
Pages (from-to)	919-924
Journal	JACC Case Rep
Volume	2
Issue number	6
DOIs	https://doi.org/10.1016/j.jaccas.2020.01.006
Publication status	Published - Jun 2020

Keywords

arrhythmogenic cardiomyopathy
arrhythmogenic right ventricular cardiomyopathy
deformation imaging
desmosomal mutations
genetic screening
pediatrics
ventricular tachycardia

Access to Document

10.1016/j.jaccas.2020.01.006

1-s2.0-S2666084920300255-mainFinal published version, 1.77 MBLicence: CC BY-NC-ND

Cite this

@article{44636214da074d73bb17149e54478277,

title = "Arrhythmogenic Right Ventricular Cardiomyopathy in a Pediatric Patient Case Report: Clinical Case",

abstract = "Arrhythmogenic right ventricular cardiomyopathy (ARVC) is rarely diagnosed in childhood. We describe the case of a 9-year-old girl with genetically confirmed ARVC who presented with syncope, ventricular arrhythmia, and biventricular myocardial dysfunction. This case highlights the need for development of pediatric ARVC diagnosis criteria specific for pediatric patients and discusses potential diagnostic improvement using echocardiographic deformation imaging. (Level of Difficulty: Beginner.)",

keywords = "arrhythmogenic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, deformation imaging, desmosomal mutations, genetic screening, pediatrics, ventricular tachycardia",

author = "Rob Roudijk and R. Evertz and Arco Teske and C. Marcelis and Bosboom, \{Dennis G H\} and BK Velthuis and \{Udink ten Cate\}, F.E.A. and \{te Riele\}, \{Anneline S.J.M.\}",

year = "2020",

month = jun,

doi = "10.1016/j.jaccas.2020.01.006",

language = "English",

volume = "2",

pages = "919--924",

journal = "JACC Case Rep",

issn = "2666-0849",

publisher = "Elsevier",

number = "6",

}

TY - JOUR

T1 - Arrhythmogenic Right Ventricular Cardiomyopathy in a Pediatric Patient Case Report: Clinical Case

AU - Roudijk, Rob

AU - Evertz, R.

AU - Teske, Arco

AU - Marcelis, C.

AU - Bosboom, Dennis G H

AU - Velthuis, BK

AU - Udink ten Cate, F.E.A.

AU - te Riele, Anneline S.J.M.

PY - 2020/6

Y1 - 2020/6

N2 - Arrhythmogenic right ventricular cardiomyopathy (ARVC) is rarely diagnosed in childhood. We describe the case of a 9-year-old girl with genetically confirmed ARVC who presented with syncope, ventricular arrhythmia, and biventricular myocardial dysfunction. This case highlights the need for development of pediatric ARVC diagnosis criteria specific for pediatric patients and discusses potential diagnostic improvement using echocardiographic deformation imaging. (Level of Difficulty: Beginner.)

AB - Arrhythmogenic right ventricular cardiomyopathy (ARVC) is rarely diagnosed in childhood. We describe the case of a 9-year-old girl with genetically confirmed ARVC who presented with syncope, ventricular arrhythmia, and biventricular myocardial dysfunction. This case highlights the need for development of pediatric ARVC diagnosis criteria specific for pediatric patients and discusses potential diagnostic improvement using echocardiographic deformation imaging. (Level of Difficulty: Beginner.)

KW - arrhythmogenic cardiomyopathy

KW - arrhythmogenic right ventricular cardiomyopathy

KW - deformation imaging

KW - desmosomal mutations

KW - genetic screening

KW - pediatrics

KW - ventricular tachycardia

U2 - 10.1016/j.jaccas.2020.01.006

DO - 10.1016/j.jaccas.2020.01.006

M3 - Article

SN - 2666-0849

VL - 2

SP - 919

EP - 924

JO - JACC Case Rep

JF - JACC Case Rep

IS - 6

ER -

Arrhythmogenic Right Ventricular Cardiomyopathy in a Pediatric Patient Case Report: Clinical Case

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this