SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test
Introduction
The SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the SLC52A1 gene, which is crucial for riboflavin transport in the body. This test is significant for diagnosing riboflavin deficiency, a condition that can lead to severe metabolic disorders if left untreated. By utilizing Next-Generation Sequencing (NGS) technology, this test provides comprehensive insights into the genetic factors contributing to riboflavin deficiency.
What the Test Measures
This genetic test detects mutations in the SLC52A1 gene that may result in impaired riboflavin absorption. Riboflavin, also known as vitamin B2, is essential for various bodily functions, including energy production and cellular function. The test can help determine if a patient is predisposed to riboflavin deficiency based on their genetic makeup.
Who Should Consider This Test
Individuals who exhibit symptoms of riboflavin deficiency, such as:
- Fatigue
- Skin disorders
- Eye problems
- Neurological issues
Moreover, those with a family history of metabolic disorders or riboflavin deficiency should consider this test to understand their genetic risks better.
Benefits of Taking the Test
- Accurate diagnosis of riboflavin deficiency.
- Early detection can lead to timely intervention and management.
- Helps in understanding genetic predispositions to metabolic disorders.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test will indicate whether any mutations were detected in the SLC52A1 gene. A genetic counselor will help interpret the results, guiding you on the next steps and potential treatments if necessary.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
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.
Book Your Test Today!
We have branches across Kenya, including Nairobi, Mombasa, Kisumu, and more. To book the SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
