Give Your Newborn the Healthiest Start with Advanced Genetic Screening
As new parents in South Africa, you naturally worry about your baby’s health and future. What if you could gain early insights into potential genetic conditions before symptoms appear? Our Newborn Genetic Screening Panel provides that peace of mind, using cutting-edge NGS technology to screen for over 200 genetic conditions that could impact your child’s development and wellbeing.
Understanding Your Baby’s Genetic Health
Next-Generation Sequencing (NGS) technology allows us to examine your newborn’s DNA with unprecedented accuracy. Unlike traditional tests that look for specific conditions, our comprehensive panel screens for a wide range of genetic disorders including metabolic conditions, developmental delays, and inherited diseases. The simple sample collection – just one drop of blood on an FTA card – makes the process stress-free for both you and your baby.
Who Should Consider Newborn Genetic Testing?
This test is particularly valuable for families with:
- History of genetic disorders in the family
- Previous children with developmental or metabolic conditions
- Consanguineous marriages (marriages between relatives)
- Unexplained infant health concerns
- Parents wanting comprehensive health screening beyond standard newborn tests
Even without family history, many South African parents choose this test for the reassurance and early intervention opportunities it provides.
Why Early Genetic Detection Matters for Your Baby
Early detection through genetic screening can be life-changing:
- Early Intervention: Identify conditions before symptoms develop, allowing for timely treatment
- Peace of Mind: Reduce anxiety about unknown genetic risks
- Informed Healthcare: Work with your paediatrician to create personalised health plans
- Family Planning: Understand genetic risks for future pregnancies
- Cost Savings: Prevent expensive late-diagnosis treatments through early detection
Understanding Your Baby’s Results
Our genetic counsellors provide clear, compassionate explanations of your results:
- Normal Results: Reassurance that no tested conditions were detected
- Carrier Status: Information about conditions your baby may carry but not develop
- Positive Findings: Early detection of conditions with guidance on next steps
- Genetic Counselling: Professional support to understand implications and create action plans
Remember: A positive result doesn’t mean your child will definitely develop the condition – it means you have valuable information to work with healthcare providers.
Investment in Your Baby’s Health Future
| Service | Regular Price | Special Price |
|---|---|---|
| Newborn Genetic Screening Panel | ZAR 10,000 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Consider this: Early detection of just one condition could save thousands in future medical costs while giving your child the best possible start.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Board-certified genetic counsellors and paediatric specialists
- Advanced Technology: State-of-the-art NGS laboratory with 99.9% accuracy
- Quick Turnaround: Results in 3-4 weeks with ongoing support
- Patient-Focused: Empathetic care designed for South African families
Secure Your Baby’s Health Future Today
Don’t wait for symptoms to appear. Take proactive control of your newborn’s health with comprehensive genetic screening.
Limited Time Offer: Save ZAR 3,300 on comprehensive newborn screening. Book now to secure this special pricing.
