Genetic Background of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Time to Start Asian Registry!
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- Horie Minoru
- Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Sciences
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- Ishida Katsuya
- Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Sciences
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- Nishio Yukiko
- Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Sciences
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- Nagaoka Iori
- Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Sciences
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- Matsui Keiji
- Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Sciences
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Abstract
Arrhythmogenic right venticular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiomyopathy with a very low penetrance affecting the right ventricle (RV) and presenting palpitation and syncope due to ventricular tachycardia (VT) originating from RV. The VT can degenerate into ventricular fibrillation and sudden cardiac death. The genetic background of ARVD/C has recently been found to be heterogeneous, mainly resulting from cell adhesion abnormalities due to mutations in five different genes encoding members of the desmosome complex. In Asian countries, however, the genetic aspect of the disease has not been fully studied, although the clinical features of Asian ARVD/C patients are different from those in Western countries in the penetrance of phenotypes, relation to Brugada syndrome and link to RV outflow tract ventricular tachycardia. It is of urgent need to have a registry of Asian ARVD/C patients and to conduct a more detailed genetic survey on the candidate genes, including desomosomal ones.
Journal
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- Journal of Arrhythmia
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Journal of Arrhythmia 24 (4), 195-199, 2008
Japanese Heart Rhythm Society
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Details 詳細情報について
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- CRID
- 1390282680222188928
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- NII Article ID
- 10027080585
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- NII Book ID
- AA12059301
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- ISSN
- 18832148
- 18804276
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- Text Lang
- en
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed