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Editorial commentary: "Three steps to ACM diagnosis - is it that easy?"
Priya Bhardwaj1, Stine B Jacobsen1, Jacob Tfelt-Hansen1
1Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark; Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Arrhythmogenic cardiomyopathy (ACM) diagnosis has evolved beyond right ventricular focus. Current guidelines emphasize comprehensive morpho-functional, electrical, and genetic assessments for accurate ACM subtype identification and risk management.
Area of Science:
- Cardiology
- Genetics
- Inherited Cardiac Diseases
Background:
- Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac condition leading to ventricular arrhythmias and sudden cardiac death.
- Diagnostic criteria for ACM have evolved significantly since 1994, moving from a sole focus on right ventricular pathology to a comprehensive phenotype evaluation.
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