Novel FHL1 Mutation Associated With Hypertrophic Cardiomyopathy, Sudden Cardiac Death, and Myopathy

Novel FHL1 Mutation Associated With Hypertrophic Cardiomyopathy, Sudden Cardiac Death, and Myopathy

A 24-year-old man with muscle cramps and a family history of sudden death presented with palpitations. Electrocardiography showed signs of left ventricular hypertrophy and nonsustained ventricular tachycardia, and imaging studies confirmed hypertrophic cardiomyopathy. Genetic testing revealed a nove...

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Bibliographic Details
Main Authors: M. Scott Binder, MD, Emily Brown, MGC, CGC, Thomas Aversano, MD, Kathryn R. Wagner, MD, PhD, Hugh Calkins, MD, Andreas S. Barth, MD, PhD
Format: Article
Language:English
Published: Elsevier 2020-03-01
Series:JACC: Case Reports
Subjects:
cardiomyopathy
chest pain
congenital heart defect
electrophysiology
genetic disorders
Online Access:http://www.sciencedirect.com/science/article/pii/S2666084919306692

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