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TTN Gene Cardiomyopathy familial hypertrophic type 9 Genetic Test Cost

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

-21%

The TTN Gene Cardiomyopathy familial hypertrophic type 9 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the TTN gene, which are implicated in familial hypertrophic cardiomyopathy type 9 (FHC9). This condition is a form of heart disease characterized by the thickening of the heart’s muscle tissue, leading to a range of symptoms from shortness of breath to heart failure. The TTN gene plays a crucial role in the structure and function of heart muscle, and mutations in this gene can disrupt heart muscle’s normal operation, contributing to the development of hypertrophic cardiomyopathy.

The test, priced at 4400 AED, involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic anomalies in the TTN gene. This test is critical for individuals with a family history of hypertrophic cardiomyopathy or related symptoms, as it can provide essential insights into the risk of developing the condition, inform treatment decisions, and guide family planning. Early detection through genetic testing like the TTN Gene Cardiomyopathy familial hypertrophic type 9 Genetic Test can significantly impact the management and prognosis of familial hypertrophic cardiomyopathy, offering a targeted approach to care and surveillance for affected individuals and their families.

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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.