TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test
Introduction
The TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test is an advanced diagnostic tool that helps identify genetic mutations associated with hypomagnesemia type 1. This condition is characterized by low magnesium levels in the body, leading to various health issues. Understanding your genetic predisposition can significantly aid in managing this metabolic disorder.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to detect mutations in the TRPM6 gene. By analyzing your DNA, it can provide insights into whether you are at risk for hypomagnesemia type 1, which is crucial for effective treatment planning.
Who Should Consider This Test?
Individuals who experience symptoms such as muscle cramps, fatigue, seizures, or irregular heart rhythms may benefit from this test. Additionally, those with a family history of metabolic disorders should consider undergoing the TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test to assess their genetic risk.
Benefits of Taking the Test
- Early identification of genetic predisposition to hypomagnesemia type 1.
- Personalized treatment plans based on genetic insights.
- Improved management of symptoms associated with magnesium deficiency.
- Informed family planning through genetic counseling.
Understanding Your Results
Upon completion of the test, you will receive a comprehensive report detailing any identified mutations in the TRPM6 gene. It is essential to consult with a healthcare professional to interpret the results accurately and discuss potential next steps.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test | 40000 KSh | 56000 KSh |
Booking Your Test
We have branches across Kenya and offer convenient home sample collection services. To book the TRPM6 Gene Hypomagnesemia Type 1 NGS Genetic DNA Test, call or WhatsApp us at +254711564616. Don’t wait—take charge of your health today!
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 the patient and a genetic counseling session to draw a pedigree chart of family members affected with hypomagnesemia type 1.
For more information, please consult with a general physician or a genetic specialist.