Hypertrophic Cardiomyopathy and Ventricular Arrhythmia

Author(s)	Z. BENNOUI
Country	Algeria
Abstract	Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiac disease. Its clinical presentation is heterogeneous, ranging from asymptomatic patients to sudden death in young individuals. This complication is unpredictable, and no preventive medical treatment has proven effective. We report the case of a 32-year-old individual who was admitted for poorly tolerated ventricular tachycardia (VT), which was resolved with external electrical shock. We diagnosed localized hypertrophic cardiomyopathy, confirmed by MRI. This paper outlines the patient's medical journey, highlighting the rhythm complications experienced and the various therapeutic options available.
Keywords	Hypertrophic Cardiomyopathy (HCM), Ventricular Tachycardia (VT), Magnetic Resonance Imaging (MRI), Preventive Medical Treatment, Therapeutic Options.
Field	Medical / Pharmacy
Published In	Volume 6, Issue 3, May-June 2024
Published On	2024-05-07
Cite This	Hypertrophic Cardiomyopathy and Ventricular Arrhythmia - Z. BENNOUI - IJFMR Volume 6, Issue 3, May-June 2024. DOI 10.36948/ijfmr.2024.v06i03.19670
DOI	https://doi.org/10.36948/ijfmr.2024.v06i03.19670
Short DOI	https://doi.org/gttbdv

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