TRPV4 Gene CMT2C NGS Genetic DNA Test
Introduction
The TRPV4 Gene CMT2C NGS Genetic DNA Test is a vital diagnostic tool that helps in identifying genetic mutations associated with Charcot-Marie-Tooth disease type 2C (CMT2C), a hereditary neurological disorder. This test employs Next-Generation Sequencing (NGS) technology to provide precise insights into your genetic makeup, which can significantly influence your health management and treatment options.
What the Test Measures
This genetic test specifically detects mutations in the TRPV4 gene, which are linked to the development of neurological disorders, particularly CMT2C. By analyzing your DNA, the test can reveal whether you carry mutations that may predispose you to this condition.
Who Should Consider This Test
Individuals with a family history of neurological disorders, particularly those exhibiting symptoms such as muscle weakness, sensory loss, or difficulty in motor functions, should consider this test. Additionally, if you have been diagnosed with CMT or have risk factors associated with genetic predispositions, this test can provide valuable information.
Benefits of Taking the Test
- Early detection of genetic predispositions to neurological disorders.
- Informed decision-making regarding treatment and management options.
- Understanding family health history and potential risks.
- Access to genetic counseling for better health management.
Understanding Your Results
Once you receive your results, it is essential to consult with a healthcare professional or genetic counselor. They can help you understand the implications of your results, discuss possible next steps, and provide guidance on managing your health based on your genetic profile.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| TRPV4 Gene CMT2C NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the TRPV4 Gene CMT2C NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Ensure you have the clinical history of the patient who is going for the test and consider a genetic counseling session to draw a pedigree chart of family members affected with TRPV4 Gene CMT2C.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
