Understanding PHC1 Gene Microcephaly: Your Path to Clarity and Peace of Mind
When you’re concerned about microcephaly running in your family, the uncertainty can feel overwhelming. We understand the anxiety that comes with not knowing whether your child might inherit this condition. Our PHC1 Gene Microcephaly Autosomal Recessive Type 11 NGS Genetic DNA Test provides the definitive answers you need to make informed decisions about your family’s health future.
What This Test Detects: Clear Answers About PHC1 Gene Mutations
This advanced genetic test specifically identifies mutations in the PHC1 gene, which is responsible for autosomal recessive microcephaly type 11. Using Next-Generation Sequencing (NGS) technology – the gold standard in genetic testing – we analyse your DNA with 99.9% accuracy to detect even the smallest genetic variations that could affect your family’s health.
Who Should Consider This Important Genetic Test?
This test is particularly important for:
- Couples with a family history of microcephaly or developmental delays
- Parents concerned about their child’s head circumference development
- Families with previous children diagnosed with neurological conditions
- Individuals planning pregnancy who want comprehensive genetic screening
- Healthcare providers seeking definitive diagnosis for patients with suspected microcephaly
If you’ve noticed developmental concerns or have family members affected by similar conditions, this test can provide the clarity you need.
Why Early Detection Matters for Your Family’s Health
Knowing your genetic status empowers you to:
- Make informed family planning decisions with confidence
- Access appropriate medical care and interventions early
- Reduce anxiety through definitive answers rather than uncertainty
- Understand inheritance patterns for future generations
- Connect with specialised healthcare providers and support networks
Early detection through genetic testing can significantly improve outcomes and provide peace of mind for your entire family.
Understanding Your Results: Clear Guidance Every Step
We know waiting for genetic results can be stressful. That’s why we provide:
- Comprehensive genetic counselling before and after testing
- Clear, easy-to-understand result explanations in plain language
- Personalised guidance on next steps based on your specific results
- Ongoing support from our genetic specialists
- Connections to appropriate medical resources if needed
Our team ensures you never feel alone in understanding what your results mean for your family.
Transparent Pricing – Exceptional Value for Peace of Mind
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| PHC1 Gene Microcephaly NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED | ||
| Family Pedigree Analysis | INCLUDED | ||
Your investment includes the complete testing process, genetic counselling, and comprehensive result analysis.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Led by certified genetic specialists and paediatric consultants
- Advanced Technology: Using NGS – the most accurate genetic testing method available
- Complete Confidentiality: Your genetic information is protected with strict privacy protocols
- Proven Accuracy: 99.9% detection rate for PHC1 gene mutations
- Quick Turnaround: Results in 3-4 weeks with ongoing support
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about microcephaly affect your family planning decisions. Our special pricing of ZAR 6,700 makes this crucial testing accessible while providing the highest standard of care.
Sample Collection Made Easy: We accept blood samples, extracted DNA, or simple blood drops on FTA cards – whatever is most convenient for you.
Limited Time Offer: Secure your special price of ZAR 6,700 before this promotion ends. Early detection provides the best opportunity for proactive health management.
Contact Oracle Genomics today and take control of your family’s genetic health journey with confidence and compassion.
