SCN5A Gene Brugada Syndrome Type 1 Genetic Test sale cost 4400 AED
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SCN5A Gene Brugada Syndrome Type 1 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

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The SCN5A gene Brugada Syndrome Type 1 genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the SCN5A gene, which are closely associated with Brugada Syndrome Type 1. This condition is a rare but serious heart rhythm disorder that can lead to sudden cardiac arrest, often in individuals without any underlying heart disease. The test is critical for individuals with a family history of Brugada Syndrome or unexplained sudden cardiac events, as it can help in the early detection and management of the condition.

The testing process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any genetic variations in the SCN5A gene that may predispose an individual to Brugada Syndrome Type 1. The results of this test can provide valuable information for personalized treatment plans and preventive measures for affected individuals and their families.

The cost of the SCN5A gene Brugada Syndrome Type 1 genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis and detailed reporting necessary to understand an individual’s genetic risk for this potentially life-threatening condition. Given the complexity and importance of the test, individuals considering this testing should consult with a healthcare professional or genetic counselor to fully understand the implications of the test results for themselves and their family members.

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SCN5A Gene Brugada syndrome type 1 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Cardiovascular Pneumology Disorders

Doctor: Cardiologist

Test Department: Genetics

Pre Test 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

Test Details

The SCN5A gene is a gene that codes for a protein called the cardiac sodium channel. Mutations in this gene have been associated with Brugada syndrome, which is a rare genetic disorder that affects the electrical system of the heart. Brugada syndrome can cause abnormal heart rhythms and can lead to sudden cardiac arrest or death.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of Brugada syndrome type 1, NGS genetic testing can be used to identify mutations in the SCN5A gene. This test involves sequencing the DNA of the individual to look for any variations or mutations in the SCN5A gene that may be associated with Brugada syndrome type 1.

By identifying these mutations, NGS genetic testing can help in the diagnosis of Brugada syndrome type 1 and also provide information about the risk of developing the condition for family members. This information can be used for genetic counseling and to guide treatment decisions for individuals with Brugada syndrome type 1.

Test Name SCN5A Gene Brugada syndrome type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test 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
Test Details

The SCN5A gene is a gene that codes for a protein called the cardiac sodium channel. Mutations in this gene have been associated with Brugada syndrome, which is a rare genetic disorder that affects the electrical system of the heart. Brugada syndrome can cause abnormal heart rhythms and can lead to sudden cardiac arrest or death.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of Brugada syndrome type 1, NGS genetic testing can be used to identify mutations in the SCN5A gene. This test involves sequencing the DNA of the individual to look for any variations or mutations in the SCN5A gene that may be associated with Brugada syndrome type 1.

By identifying these mutations, NGS genetic testing can help in the diagnosis of Brugada syndrome type 1 and also provide information about the risk of developing the condition for family members. This information can be used for genetic counseling and to guide treatment decisions for individuals with Brugada syndrome type 1.

SKU: TEST-3336 Category:

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