HCN4 Gene Brugada Syndrome Type 8 Genetic Test – DNA Labs UAE
At DNA Labs UAE, we offer the HCN4 Gene Brugada Syndrome Type 8 Genetic Test. This test is designed to analyze the HCN4 gene associated with Brugada syndrome type 8, a rare genetic disorder affecting the heart’s electrical system.
Test Components and Price
The HCN4 Gene Brugada Syndrome Type 8 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
Once the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously.
Test Type and Doctor
The HCN4 Gene Brugada Syndrome Type 8 Genetic Test falls under the category of Cardiovascular Pneumology Disorders. This test is performed by our experienced cardiologists in the Genetics department.
Pre Test Information
Prior to undergoing the HCN4 Gene Brugada Syndrome Type 8 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 the HCN4 Gene Brugada Syndrome Type 8 NGS Genetic DNA Test gene HCN4.
Test Details
Brugada syndrome type 8 is a rare genetic disorder that can cause abnormal heart rhythms and increase the risk of sudden cardiac arrest. The HCN4 Gene Brugada Syndrome Type 8 Genetic Test utilizes NGS to analyze the HCN4 gene and identify any mutations or variations associated with this condition. This test provides detailed information about an individual’s genetic makeup, aiding in the diagnosis and management of Brugada syndrome type 8.
By analyzing the HCN4 gene through NGS, our doctors can identify specific mutations or variations that may be causing Brugada syndrome type 8. This information is crucial in guiding treatment decisions, such as medication usage or the implantation of a pacemaker or defibrillator, to effectively manage the condition and reduce the risk of complications.
It is important to note that genetic testing, including NGS, should always be performed under the guidance of a healthcare professional or genetic counselor. These experts can interpret the results and provide appropriate counseling and recommendations based on the individual’s specific situation.
Test Name | HCN4 Gene Brugada syndrome type 8 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 HCN4 Gene Brugada syndrome type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HCN4 Gene Brugada syndrome type 8 NGS Genetic DNA Test gene HCN4 |
Test Details |
The HCN4 gene is associated with Brugada syndrome type 8, which is a rare genetic disorder that affects the heart’s electrical system. Brugada syndrome can cause abnormal heart rhythms and increase the risk of sudden cardiac arrest. NGS (Next-Generation Sequencing) is a type of genetic test that can analyze multiple genes simultaneously to identify any mutations or variations that may be associated with a particular condition, such as Brugada syndrome type 8. This test can provide detailed information about the genetic makeup of an individual and help in the diagnosis and management of the condition. By analyzing the HCN4 gene through NGS, doctors can identify any specific mutations or variations in the gene that may be causing Brugada syndrome type 8. This information can then be used to guide treatment decisions, such as the use of medication or implantation of a pacemaker or defibrillator, to manage the condition and reduce the risk of complications. It is important to note that genetic testing, including NGS, should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and recommendations based on the individual’s specific situation. |