Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges

doi:10.4330/wjc.v6.i12.1234

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783

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249

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Dec 26, 2014 (publication date) through Dec 16, 2024

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World Journal of Cardiology

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1949-8462

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Cardiol. Dec 26, 2014; 6(12): 1234-1244
Published online Dec 26, 2014. doi: 10.4330/wjc.v6.i12.1234

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Figure 1 Gross anatomic specimens in a patient affected by arrhythmogenic right ventricular cardiomyopathy who died suddenly. Severe right ventricular enlargement and wall atrophy and fatty replacement are evident.

Citation: Pinamonti B, Brun F, Mestroni L, Sinagra G. Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges. World J Cardiol 2014; 6(12): 1234-1244
URL: https://www.wjgnet.com/1949-8462/full/v6/i12/1234.htm
DOI: https://dx.doi.org/10.4330/wjc.v6.i12.1234