TTN Gene Cardiomyopathy Familial Hypertrophic Type 9 Genetic Test
Test Name: TTN Gene Cardiomyopathy Familial Hypertrophic Type 9 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 TTN Gene Cardiomyopathy, familial hypertrophic type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TTN Gene Cardiomyopathy, familial hypertrophic type 9 NGS Genetic DNA Test gene TTN
Test Details
TTN gene cardiomyopathy, familial hypertrophic type 9 NGS genetic test is a genetic test that analyzes the TTN gene for mutations associated with familial hypertrophic cardiomyopathy (FHC) type 9. FHC is a genetic condition characterized by the thickening of the heart muscle, leading to impaired heart function. The TTN gene provides instructions for making a protein called titin, which plays a crucial role in the contraction of heart muscle cells. Mutations in the TTN gene can disrupt the normal structure and function of titin, leading to the development of FHC.
The NGS (Next-Generation Sequencing) genetic test involves sequencing the entire TTN gene to identify any mutations or variants that may be present. This test can help in diagnosing individuals with FHC and identifying family members who may be at risk of developing the condition.
Genetic testing for TTN gene cardiomyopathy can provide important information for medical management and treatment decisions. It can help guide personalized care plans, including the use of medications, lifestyle modifications, and monitoring for potential complications.
It is important to note that genetic testing should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and guidance.
Test Name | TTN Gene Cardiomyopathy familial hypertrophic type 9 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 TTN Gene Cardiomyopathy, familial hypertrophic type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TTN Gene Cardiomyopathy, familial hypertrophic type 9 NGS Genetic DNA Test gene TTN |
Test Details |
TTN gene cardiomyopathy, familial hypertrophic type 9 NGS genetic test is a genetic test that analyzes the TTN gene for mutations associated with familial hypertrophic cardiomyopathy (FHC) type 9. FHC is a genetic condition characterized by the thickening of the heart muscle, leading to impaired heart function. The TTN gene provides instructions for making a protein called titin, which plays a crucial role in the contraction of heart muscle cells. Mutations in the TTN gene can disrupt the normal structure and function of titin, leading to the development of FHC. The NGS (Next-Generation Sequencing) genetic test involves sequencing the entire TTN gene to identify any mutations or variants that may be present. This test can help in diagnosing individuals with FHC and identifying family members who may be at risk of developing the condition. Genetic testing for TTN gene cardiomyopathy can provide important information for medical management and treatment decisions. It can help guide personalized care plans, including the use of medications, lifestyle modifications, and monitoring for potential complications. It is important to note that genetic testing should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and guidance. |