Familial Hypertrophic Cardiomyopathy With Fasciculoventricular Accessory Pathway

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&...

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Detalles Bibliográficos
Autores principales: Kalra, Vikas, Akrawinthawong, Krittapoom, Kalra, Maitri, Jain, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855128/
https://www.ncbi.nlm.nih.gov/pubmed/35199016
http://dx.doi.org/10.1016/j.jaccas.2021.12.011
Descripción
Sumario: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. (Level of Difficulty: Advanced.)

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