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TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 Genetic Test Cost

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

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The TNNI3 Gene Cardiomyopathy Familial Hypertrophic Type 7 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE. This test is designed to identify mutations in the TNNI3 gene, which are known to be a cause of Familial Hypertrophic Cardiomyopathy (FHC) type 7. FHC is a condition characterized by the thickening of the heart’s muscle, which can lead to various cardiac issues, including heart failure and arrhythmias. The TNNI3 gene plays a crucial role in the heart muscle’s contraction mechanism, and mutations in this gene can disrupt normal heart function, leading to the development of hypertrophic cardiomyopathy.

The test is particularly important for individuals with a family history of hypertrophic cardiomyopathy or related symptoms, as it can provide vital information for diagnosis, treatment, and management of the condition. Additionally, it can be used for predictive testing in asymptomatic family members to assess their risk of developing the condition.

The cost of the TNNI3 Gene Cardiomyopathy Familial Hypertrophic Type 7 Genetic Test at DNA Labs UAE is 4400 AED. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the TNNI3 gene. The results from this test can help guide clinical decisions, including surveillance and preventive measures for affected individuals and their families.

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TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 Genetic Test

At DNA Labs UAE, we offer the TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 Genetic Test. This test is designed to identify mutations in the TNNI3 gene that are associated with familial hypertrophic cardiomyopathy (FHC) type 7. FHC is a genetic condition characterized by abnormal thickening of the heart muscle, which can lead to impaired heart function.

Test Details

The TNNI3 gene provides instructions for making a protein called troponin I, which plays a crucial role in regulating muscle contraction in the heart. Mutations in the TNNI3 gene can disrupt the normal function of troponin I, leading to the development of FHC. Our TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 Genetic Test uses next-generation sequencing (NGS) technology to analyze the TNNI3 gene and detect various types of mutations, including small insertions, deletions, and substitutions.

Test Components and Price

The cost of the TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 Genetic Test is AED 4400.0. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card.

Report Delivery

After the sample is received, the report will be delivered within 3 to 4 weeks.

Test Type and Doctor

The TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 Genetic Test falls under the category of Cardiovascular Pneumology Disorders. It is conducted by our experienced Cardiologist and the test is carried out in our Genetics department.

Pre Test Information

Before undergoing the TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 NGS Genetic DNA Test gene TNNI3.

Importance of the Test

The TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 Genetic Test is crucial for diagnosing FHC type 7 and providing essential information for managing and treating the condition. It can also be used for genetic counseling and family planning purposes.

Test Name TNNI3 Gene Cardiomyopathy familial hypertrophic type 7 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 TNNI3 Gene Cardiomyopathy, familial hypertrophic type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TNNI3 Gene Cardiomyopathy, familial hypertrophic type 7 NGS Genetic DNA Test gene TNNI3
Test Details

TNNI3 gene cardiomyopathy, familial hypertrophic type 7 NGS genetic test is a genetic test that is used to identify mutations in the TNNI3 gene that are associated with familial hypertrophic cardiomyopathy (FHC) type 7. FHC is a genetic condition characterized by abnormal thickening of the heart muscle, leading to impaired heart function.

The TNNI3 gene provides instructions for making a protein called troponin I, which is involved in regulating muscle contraction in the heart. Mutations in the TNNI3 gene can disrupt the normal function of troponin I, leading to the development of FHC.

The NGS (next-generation sequencing) genetic test is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes, including the TNNI3 gene. This test can detect various types of mutations, including small insertions, deletions, and substitutions, in the TNNI3 gene.

Identifying mutations in the TNNI3 gene can help in the diagnosis of FHC type 7 and provide important information for managing and treating the condition. It can also be used for genetic counseling and family planning purposes.

SKU: TEST-3406