G6PD Gene Favism Susceptibility to NGS Genetic DNA Test
Introduction to the Test
The G6PD Gene Favism Susceptibility to NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify individuals who are genetically predisposed to Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency. This condition can lead to severe health complications, particularly in individuals exposed to certain triggers such as certain medications, foods, or infections. Understanding your G6PD status is crucial for preventing potential health crises.
What the Test Measures
This test specifically measures the presence of mutations in the G6PD gene, which is responsible for producing the G6PD enzyme. A deficiency in this enzyme can result in hemolytic anemia, especially after exposure to specific triggers.
Who Should Consider This Test
Individuals who should consider the G6PD Gene Favism Susceptibility Test include:
- Those with a family history of G6PD deficiency or Favism.
- Individuals experiencing unexplained hemolytic anemia.
- Patients who may be prescribed medications known to trigger hemolysis in G6PD-deficient individuals.
Benefits of Taking the Test
By taking the G6PD Gene Favism Susceptibility to NGS Genetic DNA Test, patients can:
- Identify their risk for G6PD deficiency.
- Make informed decisions regarding medication and dietary choices.
- Prevent potential health complications associated with G6PD deficiency.
- Receive tailored medical advice based on their genetic profile.
Understanding Your Results
Results from this test will indicate whether you carry mutations associated with G6PD deficiency. It is important to discuss these results with a healthcare provider to understand their implications and to receive guidance on necessary lifestyle adjustments.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| G6PD Gene Favism Susceptibility to NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Booking the Test
To book the G6PD Gene Favism Susceptibility to NGS Genetic DNA Test, please contact us at +2348077798758 via call or WhatsApp. Our team is ready to assist you in scheduling your appointment and answering any questions you may have.
Additional Information
Turnaround time for results is typically 3 to 4 weeks. The test requires a sample type of blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history of the patient and a genetic counseling session to draw a pedigree chart of affected family members is recommended.
Specialty: General Physician | Department: Genetics | Method: NGS Technology | Disease Type: Metabolic Disorders
