Familial Hypertrophic Cardiomyopathy With Fasciculoventricular Accessory Pathway
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2022
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American English
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Elsevier
Abstract
Hypertrophic cardiomyopathy (HCM) is a common but an underdiagnosed condition. Fasciculoventricular bypass tract (FVBT) is rare. Concomitant presence of both conditions is well described in Danon disease. We report a case of familial HCM with FVBT linked to a heterozygous pathogenic variant, c.655G>C (p.Val219Leu), in the cardiac myosin binding protein C3 (MYBPC3) gene.
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Cardiac magnetic resonance, Danon disease, Electrocardiogram, Fasciculoventricular bypass tract, Hypertrophic cardiomyopathy, Implantable cardioverter-defibrillator, Lysosome-associated membrane protein 2, Cardiac myosin binding protein C3, Nonsustained ventricular tachycardia, Wolff-Parkinson-White syndrome, Accessory pathway, Hypertrophic cardiomyopathy
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Kalra V, Akrawinthawong K, Kalra M, Jain R. Familial Hypertrophic Cardiomyopathy With Fasciculoventricular Accessory Pathway. JACC Case Rep. 2022;4(4):198-204. Published 2022 Feb 16. doi:10.1016/j.jaccas.2021.12.011
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JACC Case Reports
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PMC
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Article
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