CA12 Gene Hyperchlorhidrosis Isolated NGS Genetic DNA Test
Introduction
The CA12 Gene Hyperchlorhidrosis Isolated NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify genetic predispositions to hyperchlorhidrosis. This condition, characterized by excessive sweating, can significantly impact an individual’s quality of life. Understanding your genetic makeup through this test is crucial for early diagnosis and effective management.
What the Test Measures
This test specifically measures variations in the CA12 gene, which have been linked to hyperchlorhidrosis. By analyzing your genetic material through Next-Generation Sequencing (NGS) technology, we can detect mutations that may contribute to this metabolic disorder.
Who Should Consider This Test?
Individuals experiencing symptoms of excessive sweating or those with a family history of hyperchlorhidrosis should consider this test. Risk factors include:
- Family history of hyperchlorhidrosis
- Presence of excessive sweating in daily life
- Other metabolic disorders
Benefits of Taking the Test
Taking the CA12 Gene Hyperchlorhidrosis test provides numerous benefits:
- Early identification of genetic predisposition to hyperchlorhidrosis
- Informed decision-making regarding lifestyle changes and treatments
- Access to tailored genetic counseling for affected family members
Understanding Your Results
Once the test is complete, you will receive a comprehensive report detailing the findings. It’s essential to discuss these results with your healthcare provider, who can guide you on the next steps and potential management strategies.
Pricing Information
Test Name | Discount Price | Regular Price |
---|---|---|
CA12 Gene Hyperchlorhidrosis Isolated NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test Today!
Don’t wait to take control of your health. Book the CA12 Gene Hyperchlorhidrosis Isolated NGS Genetic DNA Test today! For more information or to schedule your test, please call or WhatsApp us at +2348077798758.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A genetic counseling session to draw a pedigree chart of family members affected with hyperchlorhidrosis is recommended.