CLDN16 Gene Hypomagnesemia Type 3 NGS Genetic DNA Test
Introduction to the Test
The CLDN16 Gene Hypomagnesemia Type 3 NGS Genetic DNA Test is a groundbreaking diagnostic tool designed to detect genetic mutations associated with hypomagnesemia type 3. This condition affects magnesium levels in the body, leading to various metabolic disorders. Understanding your genetic predisposition is crucial for effective management and treatment.
What the Test Measures
This test specifically measures genetic variations in the CLDN16 gene, which plays a vital role in magnesium transport across cell membranes. By analyzing these variations, healthcare providers can determine the underlying genetic causes of hypomagnesemia.
Who Should Consider This Test
Individuals experiencing symptoms of low magnesium levels, such as muscle cramps, fatigue, and irregular heartbeats, should consider this test. Additionally, those with a family history of hypomagnesemia or related metabolic disorders may benefit from genetic testing to identify potential risks.
Benefits of Taking the Test
- Identifies genetic causes of hypomagnesemia, allowing for targeted treatment.
- Provides valuable insights into family health history.
- Facilitates informed decision-making regarding lifestyle and dietary changes.
- Helps in the early detection of potential health issues related to magnesium deficiency.
Understanding Your Results
Results from the CLDN16 Gene Hypomagnesemia Type 3 NGS Genetic DNA Test will provide insights into the presence of genetic mutations. A genetic counselor will help interpret these results, guiding you through the implications for your health and your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CLDN16 Gene Hypomagnesemia Type 3 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Booking Your Test
We have branches across all major cities in Kenya, making it easy for you to access our services. To book the CLDN16 Gene Hypomagnesemia Type 3 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Our team is ready to assist you with the booking process and provide any additional information you may need.
Additional Information
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 going for the test and a genetic counseling session to draw a pedigree chart of family members affected with Hypomagnesemia type 3.
Take charge of your health today with the CLDN16 Gene Hypomagnesemia Type 3 NGS Genetic DNA Test. Understanding your genetic makeup is the first step towards better health!
