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Arrhythmogenic right ventricular cardiomyopathy in monozygotic twin sisters, and persistent left superior vena cava in one complicating implantation of ICD. | LitMetric
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Arrhythmogenic right ventricular cardiomyopathy in monozygotic twin sisters, and persistent left superior vena cava in one complicating implantation of ICD.

Mehmet Ali Astarcıoğlu Mehmet Yaymacı Taner Şen Celal Kilit Basri Amasyalı

Turk Kardiyol Dern Ars

Department of Cardiology, Dumlupinar University Evliya Celebi Training and Research Hospital, Kutahya, Turkey.

Published: October 2015

AI Article Synopsis

  • Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetic heart condition marked by the replacement of heart muscle with fibrous and fatty tissue.
  • It leads to irregular heartbeats (ventricular arrhythmias) and problems with the right ventricle's function.
  • The report discusses identical twins affected by ARVC, indicating that a genetic issue is likely behind their condition.

Article Abstract

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized histologically by fibro-fatty replacement of heart muscle, and clinically by ventricular arrhythmias and right ventricular dysfunction. This report presents monozygotic twins with ARVC, suggesting a genetic abnormality as the most probable cause.

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 Source
http://dx.doi.org/10.5543/tkda.2015.38959DOI Listing

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