Associazione Nazionale Medici Cardiologi Ospedalieri

CONGRESS ABSTRACT

CONGRESS ABSTRACT

Categorie
A pediatric case of calcium release deficiency syndrome
Anno:
2025
Introduction: Calcium release deficiency syndrome, recently identified, is a ryanodinopathy caused by mutations in the Ryr2 gene that result in loss of function of the gene. Clinically, it is associated with the risk of polymorphic VT and sudden death. Arrhythmias are not triggered by physical activity and can occur…