SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test
Introduction
The SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test is a revolutionary diagnostic tool that identifies mutations in the SLC52A1 gene, which are responsible for riboflavin deficiency. Riboflavin, also known as vitamin B2, is essential for various metabolic processes in the body, including energy production and the metabolism of fats, drugs, and steroids. Understanding your genetic predisposition to riboflavin deficiency can lead to timely interventions and better health outcomes.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to detect specific mutations in the SLC52A1 gene. By analyzing the genetic code, healthcare providers can determine if an individual is at risk for riboflavin deficiency, which can lead to serious health issues if left untreated.
Who Should Consider This Test?
Individuals who exhibit symptoms of riboflavin deficiency such as:
- Fatigue
- Skin disorders
- Eye problems, including sensitivity to light
- Oral lesions
Additionally, those with a family history of metabolic disorders or genetic predispositions should consider this test for proactive health management.
Benefits of Taking the Test
- Early identification of genetic risks associated with riboflavin deficiency.
- Informed decision-making regarding dietary and lifestyle changes.
- Access to tailored treatment and management plans.
- Peace of mind for individuals and families regarding genetic health risks.
Understanding Your Results
Results from the SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test will provide insight into your genetic makeup concerning riboflavin metabolism. A genetic counseling session is recommended to help interpret the results and discuss potential implications for you and your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
How to Book the Test
To book the SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test, please contact us at +2348110567037 via call or WhatsApp. Our team is ready to assist you with the booking process and any questions you may have.
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 clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by riboflavin deficiency.
Don’t wait to take control of your health! Book the SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test today.
