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Start Over Descriptor "Arrhythmogenic right ventricular dysplasia/physiopathology" Topic monozygotic twins
3 results on '"Arrhythmogenic right ventricular dysplasia/physiopathology"'

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

Author

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

Subjects
arrhythmogenic right ventricular dysplasia/physiopathology, pacemaker, artificial, monozygotic twins, Medicine, Internal medicine, RC31-1245, Diseases of the circulatory (Cardiovascular) system, RC666-701
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.

Published
2015
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2. Arrhythmogenic right ventricular cardiomyopathy in monozygotic twin sisters, and persistent left superior vena cava in one complicating implantation of ICD.

Author

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

Abstract

Copyright of Archives of the Turkish Society of Cardiology / Türk Kardiyoloji Derneği Arşivi is the property of KARE Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Published
2015
Full Text
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3. Arrhythmogenic right ventricular cardiomyopathy in monozygotic twin sisters, and persistent left superior vena cava in one complicating implantation of ICD

Author

Mehmet Yaymaci, Celal Kilit, Basri Amasyali, Mehmet Ali Astarcıoğlu, and Taner Şen

Subjects
Adult, lcsh:Internal medicine, lcsh:Diseases of the circulatory (Cardiovascular) system, Superior Vena Cava Syndrome, medicine.medical_specialty, Arrhythmogenic right ventricular dysplasia/physiopathology, artificial, lcsh:Medicine, Monozygotic twin, Right ventricular cardiomyopathy, Diagnosis, Differential, Electrocardiography, Internal medicine, Diseases in Twins, medicine, Humans, Persistent left superior vena cava, cardiovascular diseases, lcsh:RC31-1245, Arrhythmogenic Right Ventricular Dysplasia, Superior vena cava syndrome, medicine.diagnostic_test, business.industry, lcsh:R, Magnetic resonance imaging, Twins, Monozygotic, medicine.disease, Magnetic Resonance Imaging, pacemaker, Defibrillators, Implantable, Arrhythmogenic right ventricular dysplasia, Pacemaker, artificial, lcsh:RC666-701, Cardiology, cardiovascular system, Female, medicine.symptom, Differential diagnosis, Cardiology and Cardiovascular Medicine, business, Monozygotic twins
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. © 2015 Turkish Society of Cardiology.

Published
2015

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