CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA (CPVT): CLINICAL EXOME PANEL (Sec. & CNVs) – 13 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
The Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) panel analyzes 13 genes associated with this inherited channelopathy characterized by ventricular arrhythmias induced by exercise or emotional stress, in the absence of structural heart disease. Using next-generation sequencing (NGS) with detection of SNVs, indels, and CNVs, it identifies variants in genes that regulate intracellular calcium handling and cardiac excitability, which are responsible for abnormal catecholaminergic depolarization.
Featured genes: RYR2, CASQ2, TRDN, CALM1, CALM2, CALM3, ANK2, KCNJ2, SCN5A, LMNA. You can consult the complete list of genes included in the panel by contacting Genotica.
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