Protect Your Newborn from Severe Jaundice with Advanced Genetic Testing
As expectant parents in South Africa, the health of your newborn is your highest priority. The UGT1A1 Gene Hyperbilirubinemia Test provides crucial early detection of genetic factors that could lead to severe neonatal jaundice, giving you the knowledge to protect your baby’s health from day one.
Understanding the UGT1A1 Gene Test
This advanced Next-Generation Sequencing (NGS) test examines the UGT1A1 gene, which plays a vital role in processing bilirubin in your baby’s body. When this gene doesn’t function properly, it can lead to familial transient neonatal hyperbilirubinemia – a condition where newborns develop dangerously high levels of bilirubin that can cause brain damage if untreated.
Our test provides clear, accurate results that help your paediatrician create a personalised monitoring and treatment plan, ensuring your newborn receives the right care at the right time.
Who Should Consider This Genetic Test?
This test is particularly important for South African families who:
- Have a family history of severe neonatal jaundice
- Are planning pregnancy and want to understand genetic risks
- Have previously had a baby with prolonged or severe jaundice
- Want comprehensive genetic information for their newborn’s health
- Are concerned about their baby’s bilirubin processing ability
Early detection through genetic testing can prevent the anxiety of unexpected health complications and ensure your baby receives appropriate monitoring from birth.
Why This Test Matters for Your Baby’s Health
Knowing your baby’s genetic risk for hyperbilirubinemia provides significant benefits:
- Early Intervention: Allows for proactive monitoring and treatment planning
- Peace of Mind: Reduces uncertainty about your newborn’s health risks
- Prevention of Complications: Helps prevent kernicterus (brain damage from high bilirubin)
- Personalised Care: Enables tailored healthcare strategies for your baby
- Family Planning Insights: Provides valuable information for future pregnancies
Understanding Your Test Results
Our comprehensive genetic counselling session helps you understand your results clearly and without medical jargon. We’ll explain:
- What the UGT1A1 gene variations mean for your baby
- Practical steps you can take with your healthcare provider
- Monitoring protocols for your newborn
- Treatment options if elevated risk is detected
- What the results mean for your family’s genetic health
You’ll leave with a clear action plan and the confidence to protect your baby’s health.
Affordable Genetic Testing for South African Families
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| UGT1A1 Gene Hyperbilirubinemia Test | ZAR 6,700 | ZAR 2,650 |
Test Details:
- Turnaround Time: 3-4 weeks
- Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
- Includes: Genetic counselling session and family pedigree analysis
- Method: Advanced NGS Technology for maximum accuracy
Why Trust Oracle Genomics?
As South Africa’s leading genetic testing provider, we offer:
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified general physicians
- Advanced Technology: State-of-the-art NGS testing for reliable results
- Comprehensive Support: Genetic counselling included with every test
- Patient-Focused Care: Empathetic support throughout your testing journey
Take the First Step Toward Protecting Your Newborn’s Health
Don’t wait until symptoms appear. Early genetic detection gives you the power to prevent serious health complications and ensure your baby gets the best possible start in life.
Limited Time Offer: Save ZAR 2,650 on this essential genetic test. Book now to secure your special pricing and give your newborn the gift of protected health.
