TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test
Introduction
The TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with Hypomagnesemia Type 1. This condition is characterized by low levels of magnesium in the blood, leading to various metabolic disorders. Understanding your genetic predisposition to this condition is crucial for timely intervention and management.
What the Test Measures
This test specifically detects mutations in the TRPM6 gene, which plays a vital role in magnesium transport within the body. By analyzing the genetic makeup, healthcare providers can determine if an individual is at risk for developing hypomagnesemia and related metabolic disorders.
Who Should Consider This Test?
Individuals who experience symptoms such as muscle cramps, fatigue, or neurological issues may benefit from this test. Additionally, those with a family history of hypomagnesemia or metabolic disorders should consider genetic testing to assess their risk factors.
Benefits of Taking the Test
- Early detection of genetic predispositions allows for proactive health management.
- Understanding your genetic risks can guide lifestyle and dietary changes.
- Facilitates informed discussions with healthcare providers about treatment options.
- Helps in family planning and understanding hereditary conditions.
Understanding Your Results
Results from the TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test will provide insights into whether any mutations were detected. A positive result indicates a higher risk for hypomagnesemia, allowing for tailored management strategies. It is essential to discuss your results with a healthcare professional for comprehensive understanding and guidance.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test today and take the first step towards better health management. For inquiries or to schedule your appointment, call or WhatsApp us at +2348110567037.
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 counselling session is recommended to draw a pedigree chart of family members affected with Hypomagnesemia Type 1.
This test falls under the specialty of General Physician and the department of Genetics, utilizing NGS Technology to provide accurate results for metabolic disorders.
