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SCN1B Gene Brugada Syndrome Type 5 Genetic Test Cost

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

-21%

The SCN1B Gene Brugada Syndrome Type 5 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SCN1B gene, which are linked to Brugada Syndrome Type 5. This condition is a rare, inherited form of heart disease that can lead to dangerous heart rhythms and, in severe cases, sudden cardiac arrest. The test plays a crucial role in the early detection and management of this syndrome, enabling healthcare providers to implement preventive measures and tailor treatments for individuals at risk. Priced at 4400 AED, this genetic test is a valuable resource for individuals with a family history of Brugada Syndrome or unexplained cardiac symptoms, offering a pathway to better health outcomes through personalized medicine.

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SCN1B Gene Brugada syndrome type 5 Genetic Test

Are you concerned about Brugada syndrome and its genetic implications? DNA Labs UAE offers the SCN1B Gene Brugada syndrome type 5 Genetic Test at a competitive price of 4400.0 AED.

Test Components and Details

  • Test Name: SCN1B Gene Brugada syndrome type 5 Genetic Test
  • 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

Prior to the SCN1B Gene Brugada syndrome type 5 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by Brugada syndrome and to discuss the implications of the SCN1B gene.

Test Details

The SCN1B gene is closely associated with Brugada syndrome, a genetic disorder affecting the heart’s electrical system. This syndrome is characterized by abnormal heart rhythms, which can lead to fainting, seizures, and, in severe cases, sudden cardiac arrest. NGS genetic testing, utilizing Next-Generation Sequencing technology, allows for the simultaneous sequencing of multiple genes.

In the case of Brugada syndrome, NGS genetic testing can identify mutations or variations in the SCN1B gene that may contribute to the condition. By analyzing the DNA sequence of the SCN1B gene, NGS genetic testing provides valuable information regarding specific mutations or variations present in an individual’s genome. This information is crucial for diagnosis, risk assessment, and treatment planning for individuals suspected or confirmed to have Brugada syndrome.

It is important to emphasize that NGS genetic testing for Brugada syndrome should be conducted and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors. These professionals can offer appropriate counseling and guidance based on the test results.

Don’t wait any longer. Contact DNA Labs UAE today to schedule your SCN1B Gene Brugada syndrome type 5 Genetic Test and gain valuable insights into your genetic health.

Test Name SCN1B Gene Brugada syndrome type 5 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 SCN1B Gene Brugada syndrome type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN1B Gene Brugada syndrome type 5 NGS Genetic DNA Test gene SCN1B
Test Details

The SCN1B gene is associated with Brugada syndrome, a genetic disorder that affects the heart’s electrical system. Brugada syndrome is characterized by abnormal heart rhythms, which can lead to fainting, seizures, and in some cases, sudden cardiac arrest.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the sequencing of multiple genes simultaneously. In the case of Brugada syndrome, NGS genetic testing can be used to identify mutations or variations in the SCN1B gene that may be responsible for the condition.

By analyzing the DNA sequence of the SCN1B gene, NGS genetic testing can provide information about the specific mutations or variations present in an individual’s genome. This information can help with diagnosis, risk assessment, and treatment planning for individuals with suspected or confirmed Brugada syndrome.

It is important to note that NGS genetic testing for Brugada syndrome should be performed and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and guidance based on the test results.

SKU: TEST-3340 Category:

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