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CACNB2 Gene Brugada Syndrome Type 4 Genetic Test Cost

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

-21%

The CACNB2 gene Brugada Syndrome Type 4 genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the CACNB2 gene, which are associated with Brugada Syndrome Type 4. Brugada Syndrome is a rare but serious condition that affects the heart’s rhythm, potentially leading to sudden cardiac arrest in otherwise healthy individuals. The test is crucial for individuals with a family history of Brugada Syndrome or unexplained cardiac symptoms, as it can help in early detection and management of the condition.

At DNA Labs UAE, the test is offered at a cost of 4400 AED. The testing process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for specific genetic alterations in the CACNB2 gene. Results from this test can provide valuable information for risk assessment, allowing healthcare providers to recommend appropriate preventive measures or interventions to reduce the risk of cardiac events associated with Brugada Syndrome Type 4.

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CACNB2 Gene Brugada Syndrome Type 4 Genetic Test

At DNA Labs UAE, we offer the CACNB2 Gene Brugada syndrome type 4 genetic test for individuals who suspect they may have this rare genetic disorder. Brugada syndrome affects the heart’s electrical system, leading to abnormal heart rhythms and an increased risk of sudden cardiac arrest.

Test Details

The CACNB2 gene is associated with Brugada syndrome type 4. To diagnose this condition, we use NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes. This advanced sequencing method quickly sequences large amounts of DNA or RNA.

Test Components and Price

The CACNB2 Gene Brugada syndrome type 4 genetic test is priced at AED 4400.0. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card. The report will be delivered within 3 to 4 weeks.

Test Type and Doctor

This test falls under the category of Cardiovascular Pneumology Disorders and is conducted by a cardiologist in our Genetics department.

Pre Test Information

Prior to the test, we require the clinical history of the patient who is undergoing the CACNB2 Gene Brugada syndrome type 4 NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the gene CACNB2.

Who Should Take the Test?

Genetic testing for Brugada syndrome, including the CACNB2 gene, is typically recommended for individuals with a suspected or confirmed diagnosis of the syndrome or for individuals with a family history of the condition. The results of genetic testing should be interpreted by a healthcare professional or genetic counselor specializing in cardiovascular genetics.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule your CACNB2 Gene Brugada syndrome type 4 genetic test.

Test Name CACNB2 Gene Brugada syndrome type 4 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 CACNB2 Gene Brugada syndrome type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CACNB2 Gene Brugada syndrome type 4 NGS Genetic DNA Test gene CACNB2
Test Details

The CACNB2 gene is associated with Brugada syndrome type 4. Brugada syndrome is a rare genetic disorder that affects the heart’s electrical system, leading to abnormal heart rhythms and an increased risk of sudden cardiac arrest.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes. It uses advanced sequencing technologies to rapidly sequence large amounts of DNA or RNA.

In the context of Brugada syndrome type 4, NGS genetic testing can be used to analyze the CACNB2 gene for any genetic variations or mutations that may be associated with the condition. This can help in the diagnosis of Brugada syndrome and in determining the appropriate treatment and management strategies for individuals with this condition.

It is important to note that genetic testing for Brugada syndrome, including the CACNB2 gene, is typically recommended for individuals with a suspected or confirmed diagnosis of the syndrome or for individuals with a family history of the condition. The results of genetic testing should be interpreted by a healthcare professional or genetic counselor who specializes in cardiovascular genetics.