LONG QT SYNDROME: CLINICAL EXOME PANEL (Sec. & CNVs) – 32 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
The Long QT Syndrome (LQTS) panel analyzes 32 genes associated with this inherited cardiac channelopathy characterized by QT interval prolongation, predisposition to ventricular tachyarrhythmias, and risk of sudden death, especially in young people and athletes. Using next-generation sequencing (NGS) with detection of SNVs, indels, and CNVs, the study identifies variants in genes encoding potassium, sodium, and calcium channels, as well as proteins that modulate cardiac repolarization.
Featured genes: KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, CALM1, CALM2, CACNA1C, RYR2, ANK2. You can consult the complete list of genes included in the panel by contacting Genotica.
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