Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel
Normaler Preis
€29.00 EUR
Normaler Preis
Verkaufspreis
€29.00 EUR
Grundpreis
pro
Verfügbarkeit für Abholungen konnte nicht geladen werden
This product is only meant for customers who already purchased a MyGenome 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.
List of main conditions:
Vollständige Details anzeigen
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
Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.