Find Answers for Unexplained Neurological Symptoms with SLC52A1 Riboflavin Deficiency Testing
When you’re experiencing mysterious symptoms that doctors struggle to diagnose, it can feel isolating and frightening. The SLC52A1 Gene Riboflavin Deficiency NGS Genetic DNA Test provides the clarity you need to understand your body’s unique challenges and take proactive steps toward better health.
Understanding Your SLC52A1 Riboflavin Deficiency Test
This advanced genetic test examines the SLC52A1 gene, which plays a crucial role in transporting riboflavin (vitamin B2) throughout your body. When this gene doesn’t function properly, your cells can’t absorb enough riboflavin, leading to progressive neurological symptoms that often go misdiagnosed for years.
Using Next Generation Sequencing (NGS) technology, we analyse your DNA with 99.9% accuracy to identify any mutations that might be affecting your riboflavin absorption. This isn’t just another test – it’s a pathway to understanding the root cause of your health concerns.
Who Should Consider This Test?
If you’re experiencing any of these symptoms, this test could provide life-changing answers:
- Unexplained neurological symptoms like muscle weakness or coordination problems
- Chronic fatigue that doesn’t improve with rest
- Developmental delays in children
- Vision problems or hearing loss without clear cause
- Family history of similar neurological conditions
- Multiple misdiagnoses without treatment success
Many patients have spent years searching for answers – our test can provide the clarity needed to move forward with targeted treatment.
Why Early Detection Matters for Your Health
Identifying SLC52A1 riboflavin deficiency early can prevent irreversible neurological damage. The good news is that this condition is treatable with high-dose riboflavin supplementation once diagnosed. Benefits of early detection include:
- Prevention of progressive neurological deterioration
- Improved quality of life through targeted treatment
- Peace of mind knowing the exact cause of symptoms
- Better management of existing symptoms
- Informed family planning decisions
- Potential to stop symptom progression
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process:
- Clear, Easy-to-Understand Reports: Your results come with plain-language explanations
- Genetic Counselling Included: Professional guidance to help you understand your results
- Personalised Recommendations: Actionable steps based on your specific genetic profile
- Family History Analysis: We help create a pedigree chart to understand inheritance patterns
Your results will clearly indicate whether SLC52A1 mutations are present and provide guidance on next steps for treatment and management.
Affordable Genetic Testing with Clear Pricing
| Test Option | Price | Savings |
|---|---|---|
| Special Price | ZAR 6,700 | ZAR 2,650 off regular price |
| Regular Price | ZAR 9,350 | – |
Includes genetic counselling session and comprehensive results analysis
Considering the cost of ongoing specialist visits, misdiagnoses, and untreated symptoms, this test represents excellent value for your health investment.
Test Details & Process
- Turnaround Time: 3 to 4 weeks
- Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
- Preparation: Clinical history and genetic counselling session to create family pedigree chart
- Technology: Next Generation Sequencing (NGS) for maximum accuracy
- Specialty: General Physician recommended
Why Trust Oracle Genomics?
We understand that genetic testing requires complete confidence in your provider. That’s why we’ve built our reputation on:
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by qualified healthcare professionals
- Proven Accuracy: 99.9% accuracy rate with NGS technology
- Patient-First Approach: Empathetic support throughout your testing journey
- Comprehensive Care: From testing to treatment guidance
Take the First Step Toward Answers Today
Don’t let unexplained symptoms control your life any longer. Early detection of SLC52A1 riboflavin deficiency can prevent permanent damage and open doors to effective treatment.
Book your test now while the special price of ZAR 6,700 is available. Our team is ready to guide you through the process with compassion and expertise.
Limited special pricing available – secure your test today to avoid missing out on ZAR 2,650 savings.
