Protect Your Newborn from Hidden Bleeding Risks
As expectant parents in South Africa, the thought of your newborn facing unexpected health challenges can be overwhelming. The ITGB3 Gene Thrombocytopenia test provides the reassurance you need by identifying potential bleeding disorders before they become emergencies. This advanced genetic screening helps ensure your baby’s first moments are safe and protected.
Understanding the ITGB3 Thrombocytopenia Test
This specialised DNA test examines the ITGB3 gene, which plays a crucial role in platelet function and blood clotting. When this gene contains mutations, it can lead to neonatal alloimmune thrombocytopenia (NAIT) – a condition where a mother’s antibodies attack her baby’s platelets, causing dangerously low platelet counts and bleeding risks.
Using cutting-edge Next Generation Sequencing (NGS) technology, we analyse your DNA with exceptional precision to detect even the smallest genetic variations that could impact your newborn’s health.
Who Should Consider This Vital Screening?
This test is particularly important for:
- Families with a history of unexplained bleeding disorders in newborns
- Parents who have experienced previous pregnancies with bleeding complications
- Couples from communities with higher genetic predisposition to blood disorders
- Expectant mothers with known platelet antibody concerns
- Families planning pregnancy who want comprehensive genetic screening
Early detection allows your medical team to prepare appropriate delivery protocols and immediate neonatal care if needed.
Why This Test Matters for Your Family’s Health
By identifying ITGB3 gene mutations early, you gain:
- Peace of Mind: Know your baby’s bleeding risk before delivery
- Delivery Planning: Enable your obstetrician to plan the safest delivery method
- Immediate Treatment: Allow neonatal specialists to be prepared with appropriate interventions
- Family Planning: Understand genetic risks for future pregnancies
- Prevention: Potentially prevent intracranial bleeding and other serious complications
Understanding Your Test Results
Our comprehensive genetic counselling ensures you fully understand your results and their implications. We provide:
- Clear, easy-to-understand result explanations
- Personalised consultation with genetic specialists
- Family pedigree analysis to understand inheritance patterns
- Guidance on next steps and management options
- Ongoing support throughout your pregnancy journey
Remember: A positive result doesn’t mean certain complications – it means you’re empowered with knowledge to ensure the best possible care.
Investment in Your Newborn’s Health
| Test Feature | Details | Value |
|---|---|---|
| Regular Price | ZAR 9,350 | Comprehensive genetic analysis |
| Special Price | ZAR 6,700 | Save ZAR 2,650 |
| Turnaround Time | 3-4 Weeks | Timely results for pregnancy planning |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | Convenient collection options |
Consider this: The cost of emergency neonatal care for bleeding complications can far exceed this preventive screening investment.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Specialist hematologists and genetic counsellors
- Advanced Technology: State-of-the-art NGS sequencing for 99.9% accuracy
- Patient-Centred Care: Empathetic support throughout your testing journey
- Proven Track Record: Trusted by healthcare providers nationwide
Take the First Step Toward Protecting Your Newborn
Don’t leave your baby’s health to chance. Early detection through genetic screening provides the knowledge you need for a safe delivery and healthy start to life.
Book your test today and secure the special price of ZAR 6,700
Available booking options:
- Online consultation and booking
- Direct clinic visits in major cities
- Telehealth genetic counselling sessions
- Partner hospital referrals
Limited time special pricing – secure your family’s peace of mind now
