Short Description

NGS genetic DNA test detecets for variant and mutation detection in SCN5A gene for Brugada syndrome type 1

PreTest Information

Clinical History of Patient who is going for SCN5A Gene Brugada syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN5A Gene Brugada syndrome type 1 NGS Genetic DNA Test gene SCN5A

Detail Description

SCN5A Gene Brugada Syndrome Type 1 NGS Genetic DNA Test

Brugada Syndrome is a rare genetic heart disorder that can cause sudden death due to abnormal heart rhythms. The SCN5A gene is responsible for the production of a protein called Nav1.5, which plays a crucial role in the normal functioning of the heart. Mutations in the SCN5A gene can lead to the development of Brugada Syndrome Type 1, which is the most common form of the disorder.

Symptoms of Brugada Syndrome Type 1

Brugada Syndrome Type 1 is characterized by an abnormal electrocardiogram (ECG) reading, which can lead to irregular heartbeats or arrhythmias. Some of the common symptoms associated with Brugada Syndrome Type 1 include:

• Heart palpitations
• Fainting or loss of consciousness
• Dizziness or lightheadedness
• Shortness of breath
• Chest pain

Diagnosis of Brugada Syndrome Type 1

Diagnosing Brugada Syndrome Type 1 can be challenging, as the symptoms may not be present all the time. An ECG can help detect the characteristic abnormalities associated with the disorder, but it may not always be conclusive. Genetic testing can help confirm the presence of the SCN5A gene mutation and aid in the diagnosis of Brugada Syndrome Type 1.

NGS Genetic DNA Test for Brugada Syndrome Type 1

The Next-Generation Sequencing (NGS) Genetic DNA Test is a highly advanced and accurate diagnostic tool that can detect genetic mutations associated with Brugada Syndrome Type 1. The test analyzes the entire sequence of the SCN5A gene and can identify even the smallest mutations that may be missed by other testing methods.

Cost of NGS Genetic DNA Test for Brugada Syndrome Type 1

The cost of the NGS Genetic DNA Test for Brugada Syndrome Type 1 is INR 20,000. The test is not covered by most insurance plans, and patients may have to pay out of pocket for the test.

Conclusion

Brugada Syndrome Type 1 is a serious genetic disorder that can cause sudden death due to abnormal heart rhythms. Early diagnosis and treatment can help prevent complications and improve outcomes. The NGS Genetic DNA Test is a highly accurate and reliable diagnostic tool that can aid in the diagnosis of Brugada Syndrome Type 1. Patients who experience symptoms associated with the disorder should consult a physician and consider undergoing genetic testing to identify any mutations in the SCN5A gene.

At DNA Labs India, we offer a wide range of genetic testing services, including NGS Genetic DNA Test for Brugada Syndrome Type 1. Our team of experts is dedicated to providing high-quality and affordable diagnostic services to patients across India. Contact us today to learn more about our services.

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 SCN5A Gene Brugada syndrome type 1 NGS Genetic DNA Test