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

Astarcıoğlu, Mehmet Ali; Yaymacı, Mehmet; Şen, Taner; Kilit, Celal; Amasyalı, Basri

Journal Metrics

Impact Factor (2025): 0.6
Scopus: Q3
CiteScore (2024): 1.1
Source Normalized Impact
per Paper:
0.315
SCImago Journal Rank: 0.250

54/3Current Issue Ahead of Print Archive Most Accessed Articles

Quick Search

In authors and

In titles and abstracts

In keywords

In all

Arrhythmogenic right ventricular cardiomyopathy in monozygotic twin sisters, and persistent left superior vena cava in one complicating implantation of ICD [Turk Kardiyol Dern Ars]

Turk Kardiyol Dern Ars. 2015; 43(7): 644-647 | DOI: 10.5543/tkda.2015.38959

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
Department of Cardiology, Dumlupınar University Evliya Celebi Training And Research Hospital, Kutahya, Turkey

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.

Keywords: Arrhythmogenic right ventricular dysplasia/physiopathology, pacemaker, artificial, monozygotic twins

Corresponding Author: Mehmet Ali Astarcıoğlu, Türkiye
Manuscript Language: English

CITE

Full Text PDF Download citation RIS EndNote BibTex Medlars Procite Reference Manager Send email to author Similar articles PubMed Google Scholar