GPD1L Gene Brugada Syndrome Type 2 Genetic Test
Test Name: GPD1L Gene Brugada syndrome type 2 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 GPD1L Gene Brugada syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GPD1L Gene Brugada syndrome type 2 NGS Genetic DNA Test gene GPD1L
Test Details: The GPD1L gene is associated with Brugada syndrome type 2, which is a rare genetic disorder that affects the electrical system of the heart. This syndrome can lead to abnormal heart rhythms and an increased risk of sudden cardiac arrest.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced technology to rapidly sequence large amounts of DNA. In the context of Brugada syndrome type 2, NGS genetic testing can be used to analyze the GPD1L gene and identify any genetic variations or mutations that may be present.
By identifying specific genetic variations in the GPD1L gene, NGS genetic testing can help diagnose Brugada syndrome type 2 and determine the risk of developing abnormal heart rhythms. This information can be used to guide treatment decisions and provide genetic counseling to affected individuals and their families.
It’s important to note that NGS genetic testing is typically performed by healthcare professionals and genetic counselors who specialize in genetic testing and interpretation. The results of the test should be discussed with a healthcare provider to fully understand the implications and potential treatment options.
Test Name | GPD1L Gene Brugada syndrome type 2 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 GPD1L Gene Brugada syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GPD1L Gene Brugada syndrome type 2 NGS Genetic DNA Test gene GPD1L |
Test Details |
The GPD1L gene is associated with Brugada syndrome type 2, which is a rare genetic disorder that affects the electrical system of the heart. This syndrome can lead to abnormal heart rhythms and an increased risk of sudden cardiac arrest. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced technology to rapidly sequence large amounts of DNA. In the context of Brugada syndrome type 2, NGS genetic testing can be used to analyze the GPD1L gene and identify any genetic variations or mutations that may be present. By identifying specific genetic variations in the GPD1L gene, NGS genetic testing can help diagnose Brugada syndrome type 2 and determine the risk of developing abnormal heart rhythms. This information can be used to guide treatment decisions and provide genetic counseling to affected individuals and their families. It’s important to note that NGS genetic testing is typically performed by healthcare professionals and genetic counselors who specialize in genetic testing and interpretation. The results of the test should be discussed with a healthcare provider to fully understand the implications and potential treatment options. |