Protect Your Baby’s Future with Prenatal Hemophilia A Screening
As expectant parents in South Africa, you naturally worry about your baby’s health and wellbeing. The thought of inherited conditions like Hemophilia A can be overwhelming, but knowledge is your greatest ally. Our Prenatal Hemophilia A Common Mutation Screening offers you the clarity and confidence you need during this precious time, providing early detection that empowers you to make informed decisions for your family’s health journey.
Understanding Your Prenatal Hemophilia A Screening
Hemophilia A is an inherited bleeding disorder that affects the blood’s ability to clot properly. Our screening specifically targets the most common genetic mutations responsible for this condition – Factor VIII Intron 22 and Intron 1 inversions. Using advanced End Point PCR technology, we analyse these critical genetic markers to provide accurate, reliable results that help you understand your baby’s potential risk.
This isn’t just a test; it’s peace of mind for South African families who want to ensure they’re prepared for any health challenges that may arise.
Who Should Consider This Important Screening?
This prenatal screening is particularly important if:
- You have a family history of Hemophilia A or bleeding disorders
- Previous pregnancies involved bleeding complications
- You’re experiencing anxiety about inherited conditions
- You want comprehensive prenatal care and preparation
- Your healthcare provider recommends genetic screening
Many South African families choose this screening not because they expect problems, but because they value being prepared and informed.
Why Early Detection Matters for Your Family
Knowing your baby’s Hemophilia A status before birth provides significant advantages:
- Peace of Mind: Reduce anxiety and uncertainty about your baby’s health
- Delivery Planning: Work with your medical team to plan the safest delivery approach
- Early Intervention: Prepare for any necessary specialized care immediately after birth
- Family Preparation: Educate yourself and your family about Hemophilia A management
- Financial Planning: Understand potential future healthcare needs
Understanding Your Results with Confidence
We know waiting for genetic test results can be stressful. That’s why we provide clear, easy-to-understand reports with professional guidance. Your results will clearly indicate whether the common Hemophilia A mutations were detected, and our team is available to help you understand what this means for your pregnancy and baby’s health.
Remember: A positive result doesn’t mean certain illness – it means you have valuable information to work with your healthcare providers for the best possible outcomes.
Affordable Peace of Mind for South African Families
| Test Option | Price | Value |
|---|---|---|
| Regular Price | ZAR 6,700 | Comprehensive genetic analysis |
| Special Offer | ZAR 5,000 | Save ZAR 1,700 |
Turnaround time: 10-11 days | Sample: Peripheral blood/Amniotic Fluid/Chorionic villi/Cord blood
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Working with general physicians and specialists throughout the country
- Accuracy Commitment: Advanced End Point PCR technology ensures reliable results
- Patient-Focused Care: Empathetic support throughout your testing journey
- Proven Track Record: Trusted by healthcare providers nationwide
Take the Next Step Toward Your Baby’s Health
Don’t let uncertainty cloud your pregnancy journey. This limited-time offer of ZAR 5,000 (save ZAR 1,700) makes comprehensive prenatal screening more accessible than ever for South African families.
Limited availability at special price – secure your screening today!
Note: This test requires a doctor’s prescription (not applicable for surgery, pregnancy cases, or travel abroad planning).
