A Family with Recurrent Sudden Death and No Clinical Clue

作者：Arad Michael^*; Glikson Michael; El Ani Dalia; Monserrat Inglesias Lorenzo

来源：Annals of Noninvasive Electrocardiology, 2012, 17(4): 387-393.

DOI：10.1111/anec.12024

• Molecular biology
• genetics
• Electrophysiology - ventricular tachycardia
• Sudden death

Background: Sudden cardiac death of a child is a devastating event for the family and an enormous challenge for the attending physician. Methods and Results: We report a family with repeat events of sudden cardiac death and recurrent ventricular fibrillation in a teenage girl, where autopsy data and clinical investigations were inconclusive. The diagnosis of catecholaminergic polymorphic ventricular tachycardia (CPVT) was established only following finding a gene mutation in the cardiac ryanodine receptor. Conclusions: Interpretation of autopsy data, provocation testing and genetic testing in victims of sudden death and family members are discussed to correctly identify the cause and properly manage asymptomatic carriers in such families.

• 出版日期2012-10