FXYD2 Gene Hypomagnesemia Type 2 NGS Genetic DNA Test
The FXYD2 Gene Hypomagnesemia Type 2 NGS Genetic DNA Test is a specialized genetic test that examines the FXYD2 gene, which plays a crucial role in magnesium transport in the body. Hypomagnesemia type 2 is a metabolic disorder characterized by low magnesium levels, which can lead to severe health problems. This test is important for individuals who may have a genetic predisposition to this condition, helping to identify the underlying cause and guide treatment options.
What the Test Measures
This test specifically detects mutations in the FXYD2 gene that are associated with hypomagnesemia type 2. By analyzing the genetic material, we can determine if there are any abnormalities that could explain the patient’s symptoms.
Who Should Consider This Test
Individuals experiencing symptoms such as muscle cramps, fatigue, or irregular heartbeats should consider this test. Additionally, those with a family history of metabolic disorders or unexplained hypomagnesemia may also benefit from testing. Risk factors include a history of kidney disease or other metabolic conditions.
Benefits of Taking the Test
- Accurate diagnosis of hypomagnesemia type 2
- Guidance for treatment options and management strategies
- Informed decision-making for family planning and genetic counseling
- Understanding potential health risks associated with the condition
Understanding Your Results
Once the test is completed, results will typically be available within 3 to 4 weeks. A genetic counselor will help interpret the findings, providing insights into what the results mean for your health and any necessary next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FXYD2 Gene Hypomagnesemia Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To take the next step in understanding your health, book the FXYD2 Gene Hypomagnesemia Type 2 NGS Genetic DNA Test today. For more information or to schedule your appointment, please call or WhatsApp us at +2348110567037.
Pre-Test Instructions: Prior to the test, a clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by hypomagnesemia type 2.
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders
