Short Description

NGS genetic DNA test detecets for variant and mutation detection in CACNA1C gene for Brugada syndrome type 3

PreTest Information

Clinical History of Patient who is going for CACNA1C Gene Brugada syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CACNA1C Gene Brugada syndrome type 3 NGS Genetic DNA Test gene CACNA1C

Detail Description

CACNA1C Gene Brugada Syndrome Type 3 NGS Genetic DNA Test

Brugada Syndrome is a rare genetic condition that affects the heart's rhythm. It increases the risk of sudden cardiac arrest, which can be life-threatening. The condition is caused by mutations in the CACNA1C gene, which codes for a protein called the CaV1.2 channel. This protein is responsible for controlling the flow of calcium ions into heart cells, which is essential for proper heart function.

Symptoms of Brugada Syndrome

The symptoms of Brugada Syndrome can vary widely, but they typically include:

• Episodes of fainting or near-fainting
• Palpitations
• Shortness of breath
• Chest pain
• Abnormal heart rhythms

It's important to note that not everyone with Brugada Syndrome will experience these symptoms. In fact, some people may not even know they have the condition until they undergo testing for another reason.

Diagnosis of Brugada Syndrome

The diagnosis of Brugada Syndrome can be challenging because the symptoms can be vague and nonspecific. However, there are several tests that can be used to diagnose the condition:

• Electrocardiogram (ECG): This is a test that records the electrical activity of the heart. People with Brugada Syndrome may have characteristic changes on their ECG.
• Genetic testing: This is a test that looks for mutations in the CACNA1C gene. If a mutation is found, it can confirm a diagnosis of Brugada Syndrome.
• Provocation testing: This is a test that involves administering drugs that can reveal changes on the ECG that are characteristic of Brugada Syndrome.

CACNA1C Gene Brugada Syndrome Type 3 NGS Genetic DNA Test

The CACNA1C Gene Brugada Syndrome Type 3 NGS Genetic DNA Test is a genetic test that looks for mutations in the CACNA1C gene. This test can confirm a diagnosis of Brugada Syndrome and identify family members who may be at risk of developing the condition.

The cost of the CACNA1C Gene Brugada Syndrome Type 3 NGS Genetic DNA Test in India is INR 20,000.

Conclusion

Brugada Syndrome is a rare genetic condition that can be life-threatening. The CACNA1C Gene Brugada Syndrome Type 3 NGS Genetic DNA Test is a useful tool for diagnosing the condition and identifying at-risk family members. If you or a loved one have symptoms of Brugada Syndrome, it's important to seek medical attention right away.

Contact DNA Labs India today to schedule your CACNA1C Gene Brugada Syndrome Type 3 NGS Genetic DNA Test.