TRDN
Associated conditions:
- Catecholaminergic Polymorphic Ventricular Tachycardia
TRDN makes triadin, part of the machinery that releases calcium to power each heartbeat, working alongside the main cardiac calcium release channel. Genetic changes in this gene disrupt calcium control and are associated with an autosomal recessive form of Catecholaminergic polymorphic ventricular tachycardia (CPVT) with stress-triggered arrhythmias in children and young adults. Knowing your genetic status enables early recognition and protective treatment.
Conditions linked to TRDN
Catecholaminergic Polymorphic Ventricular Tachycardia
CPVT is an inherited rhythm disorder in which physical exertion or strong emotion can trigger a dangerously fast heartbeat. It is managed with medication and activity guidance, so a diagnosis allows protective steps before symptoms occur.
