Case report
Open access
Oct 2026
Ventricular Fibrillation in PRKAG2 Cardiomyopathy: A Genetic Arrhythmia Substrate Beyond Wolff-Parkinson-White.
BACKGROUND PRKAG2 syndrome is a rare autosomal dominant glycogen storage cardiomyopathy characterized by left ventricular hypertrophy, ventricular pre-excitation, and progressive conduction system disease. CASE SUMMARY We report the case of a 25-year-old woman with genetically confirmed PRKAG2 syndrome who presented...
Julia Visch, L. Hopman, Danny Holtus et al.
· JACC Case Reports · 0 citations