Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel


Whole Genome Sequencing 30X

This product is only meant for customers who already purchased a Dante Genome Test

Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is caused by genetic mutations that result in an uncontrolled release of calcium in heart cells, causing ventricular arrhythmias especially during physical activity or emotional stress. Calcium, in fact, is an indispensable element for muscle contraction and for this reason its release and concentration are subjected to strict control. CPVT is a serious condition, which must be promptly identified and treated.
This panel is particularly suitable for individuals at risk of CPVT, who have close relatives affected by this rare heart disease, or who have a suspected diagnosis.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.

  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • More than 5 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Catecholaminergic polymorphic ventricular tachycardia
  • Cardiac Arrhythmia, Ankyrin-B-Related
  • Long QT Syndrome

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