TPM1 Gene Cardiomyopathy Familial Hypertrophic Type 3 NGS Genetic DNA Test
Introduction
The TPM1 Gene Cardiomyopathy Familial Hypertrophic Type 3 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with hypertrophic cardiomyopathy (HCM). This condition, characterized by the thickening of the heart muscle, can lead to serious cardiovascular issues. Early detection through genetic testing is vital for effective management and treatment.
What the Test Measures
This test utilizes next-generation sequencing (NGS) technology to analyze the TPM1 gene, which plays a critical role in cardiac muscle function. By examining this gene, the test can identify mutations that may predispose individuals to familial hypertrophic cardiomyopathy.
Who Should Consider This Test?
Individuals with a family history of cardiomyopathy or those exhibiting symptoms such as:
- Shortness of breath
- Chest pain
- Heart palpitations
- Fainting spells
are encouraged to consider this test. It is especially recommended for those with relatives diagnosed with HCM.
Benefits of Taking the Test
- Early identification of genetic predisposition to hypertrophic cardiomyopathy.
- Informed decision-making regarding lifestyle and treatment options.
- Potential for family screening and genetic counseling.
- Enhanced understanding of cardiovascular health risks.
Understanding Your Results
Results from the TPM1 Gene Cardiomyopathy test will indicate whether any mutations associated with HCM are present. A genetic counseling session is recommended to discuss the implications of your results and potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| TPM1 Gene Cardiomyopathy Familial Hypertrophic Type 3 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Book Your Test Today
We have branches across Kenya and offer a convenient home sample collection service. To book your test or for more information, please call or WhatsApp us at +254711564616.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical History of Patient and a Genetic Counseling session to draw a pedigree chart of affected family members.
This test is conducted by certified cardiologists in the field of genetics, ensuring that you receive the highest standard of care and expertise.
