Title: Arrhythmogenic Right Ventricular Dysplasia is Rare –Case Report
Author: Dr Gopalakrishnan.M
DOI: http://dx.doi.org/10.18535/jmscr/v4i6.01
Abstract
Arvd is a rare form of cardiomyopathy in which the heart muscle of the right ventricle is replaced by fat /fibrous tissue. It’s an important cause of vt in children, young adults. Its predominantly affects males, 30-50% of cases have a familial distribution.
References
1. Jain R. Athletic Status and Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: From Physiological Observations To Pathological Explanation.
2. Cox Mgpj, Van Der Zwaag Pa, Van Der Werf C; Et Al. (2011). "Arrhythmogenic Right Ventricular Dysplasia/ Cardiomyopathy".
3. Thiene G, Nava A, Corrado D, Rossi L, Pennelli N. Right Ventricular Cardiomyopathy And Sudden Death In Young People. N Engl J Med. 1988; 318:129–133
4. Saffitz Je. Cell Adhesion Pathology. In: Marcus Fi, Nava A, Thiene G, Eds. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. Milan, Italy: Springer Verlag, 2007: 45–52.
5. Peters S, Trummel M. Diagnosis Of Arrhythmogenic Right Ventricular Dysplasia-Cardiomyopathy: Value Of Standard Ecg Revisited. Ann Noninvasive Electrocardiol. 2003; 8: 238–245