Find Clarity About NAGS Deficiency: Your Path to Metabolic Health Understanding
We understand the worry that comes with metabolic health concerns, especially when they affect your children or family. The uncertainty about NAGS gene mutations can be overwhelming, but you don’t have to face it alone. Our comprehensive DNA test provides the answers you need to make informed decisions about your family’s health journey.
Understanding NAGS Gene Testing
NAGS (N-acetylglutamate synthase) deficiency is a rare metabolic disorder that affects how your body processes ammonia. When the NAGS gene doesn’t function properly, it can lead to dangerous ammonia buildup in the blood. Our advanced Next-Generation Sequencing technology examines your DNA to identify mutations in the NAGS gene, giving you clear, accurate information about your genetic makeup.
The test is straightforward and requires only a small blood sample or DNA extraction. We handle everything with the care and precision your family’s health deserves.
Who Should Consider This Test?
This test is particularly important if you or your family members experience:
- Unexplained vomiting, lethargy, or irritability in infants
- Developmental delays or learning difficulties
- Family history of metabolic disorders
- Unexplained neurological symptoms
- Previous abnormal newborn screening results
- Planning for pregnancy with family history concerns
Early detection can make a significant difference in managing this condition and preventing serious complications.
Why This Test Matters for Your Family’s Health
Getting tested provides more than just answers – it gives you peace of mind and the power to take proactive steps:
- Early Intervention: Detect potential issues before symptoms become severe
- Treatment Guidance: Help your healthcare provider develop the right treatment plan
- Family Planning: Make informed decisions about future pregnancies
- Reduce Uncertainty: Replace worry with knowledge and understanding
- Prevent Complications: Avoid the serious health risks of undiagnosed NAGS deficiency
Understanding Your Results with Compassion
We know waiting for genetic test results can be stressful. That’s why we provide:
- Clear Explanations: Your results come with easy-to-understand information
- Genetic Counselling: Professional support to help you understand what your results mean
- Next Steps Guidance: Clear recommendations for follow-up care if needed
- Ongoing Support: We’re here to answer your questions throughout the process
Remember: A positive result doesn’t mean certain illness – it means you have information to work with your healthcare team for the best possible outcomes.
Affordable Peace of Mind for South African Families
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| NAGS Gene DNA Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
What’s Included: Comprehensive genetic analysis, professional genetic counselling session, detailed results report, and ongoing support.
Turnaround Time: 3-4 weeks
Sample Required: Blood, extracted DNA, or one drop of blood on FTA card
Why Trust Oracle Genomics?
We’ve built our reputation on accuracy, compassion, and reliability:
- Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Working with qualified general physicians and genetic specialists
- Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
- Patient-First Approach: Your comfort and understanding are our top priorities
- Proven Track Record: Thousands of South African families trust us with their genetic testing needs
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about NAGS deficiency control your family’s future. With our special pricing of ZAR 6,700, comprehensive genetic counselling, and nationwide availability, there’s never been a better time to get the answers you deserve.
Limited Time Offer: This special pricing won’t last forever. Secure your family’s peace of mind while you can save ZAR 2,650.
“The genetic counselling session gave us so much clarity. We finally understood what we were dealing with and could make informed decisions.” – Previous Patient
