Short Description

NGS genetic DNA test detecets for variant and mutation detection in RYR2 gene for Ventricular tachycardia, catecholaminergic polymorphic type 1

PreTest Information

Clinical History of Patient who is going for RYR2 Gene Ventricular tachycardia, catecholaminergic polymorphic type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RYR2 Gene Ventricular tachycardia, catecholaminergic polymorphic type 1 NGS Genetic DNA Test gene RYR2

Detail Description

RYR2 Gene Ventricular Tachycardia: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Ventricular tachycardia is a type of arrhythmia that originates from the ventricles of the heart. It is characterized by a fast heart rate, which can be life-threatening if not treated promptly. In some cases, ventricular tachycardia is caused by genetic mutations, such as the RYR2 gene mutation. Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare genetic disorder that affects the heart's ability to regulate heart rate and rhythm.

What is the RYR2 Gene?

The RYR2 gene is responsible for producing a protein called ryanodine receptor 2. This protein plays an important role in regulating calcium release in the heart muscle cells. Mutations in the RYR2 gene can cause abnormal calcium release, which can lead to arrhythmias like ventricular tachycardia.

What is Catecholaminergic Polymorphic Ventricular Tachycardia?

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare genetic disorder that affects the heart's ability to regulate heart rate and rhythm. It is caused by mutations in genes that control the release of calcium in the heart muscle cells. CPVT usually affects children and young adults and can be triggered by exercise or emotional stress.

Symptoms of RYR2 Gene Ventricular Tachycardia

The symptoms of RYR2 gene ventricular tachycardia can include:

• Fast heart rate
• Dizziness or lightheadedness
• Fainting or near-fainting
• Chest pain or discomfort
• Shortness of breath

Diagnosis of RYR2 Gene Ventricular Tachycardia

If you are experiencing symptoms of ventricular tachycardia, your doctor may recommend an electrocardiogram (ECG) to monitor your heart's electrical activity. They may also order other tests, such as a Holter monitor or a stress test, to help diagnose your condition. Genetic testing can also be done to check for mutations in the RYR2 gene.

NGS Genetic DNA Test Cost for RYR2 Gene Ventricular Tachycardia

The cost of NGS genetic DNA testing for RYR2 gene ventricular tachycardia can vary depending on the laboratory and the location. In India, the cost of this test can be around INR 20,000. However, it is important to note that this test may not be covered by insurance and may require out-of-pocket expenses.

Conclusion

Ventricular tachycardia can be a life-threatening condition, especially if it is caused by genetic mutations like the RYR2 gene mutation. If you are experiencing symptoms of ventricular tachycardia, it is important to see a doctor as soon as possible. Genetic testing can help diagnose the underlying cause of your condition and guide treatment options.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for RYR2 Gene Ventricular tachycardia, catecholaminergic polymorphic type 1 NGS Genetic DNA Test