Find Clarity About Treacher Collins Syndrome in Your Family
When you’re worried about inherited craniofacial conditions affecting your child or family members, the uncertainty can be overwhelming. Our POLR1C gene test provides the definitive answers you need to make informed decisions about your family’s health journey. Using cutting-edge NGS technology, we deliver accurate, reliable results that bring peace of mind and clear direction.
Understanding the POLR1C Gene Test
The POLR1C gene test is a sophisticated genetic analysis that specifically examines the POLR1C gene for mutations associated with Treacher Collins Syndrome type 3. This rare genetic condition affects facial bone development and can be inherited through families. Our Next-Generation Sequencing (NGS) technology provides comprehensive analysis of your DNA, ensuring the highest level of accuracy in detecting even subtle genetic variations.
Unlike basic genetic screenings, our test offers complete sequencing of the POLR1C gene, giving you and your healthcare providers the detailed information needed for proper diagnosis and management planning.
Who Should Consider This Genetic Test?
This test is particularly important for:
- Children showing signs of craniofacial abnormalities or developmental delays
- Families with a history of Treacher Collins Syndrome or similar conditions
- Parents planning future pregnancies who want to understand genetic risks
- Individuals with unexplained facial features that might suggest genetic origins
- Healthcare providers seeking definitive diagnosis for treatment planning
If you’ve noticed unusual facial characteristics, hearing difficulties, or developmental concerns in your child, this test can provide the clarity needed for proper medical care.
Why Early Detection Matters for Your Family’s Health
Getting accurate genetic information early can significantly impact your child’s quality of life and future health outcomes. With definitive POLR1C gene testing, you can:
- Access appropriate medical interventions and specialist care sooner
- Make informed decisions about family planning and future pregnancies
- Reduce uncertainty and anxiety about your child’s health condition
- Connect with the right support services and medical specialists
- Develop a comprehensive care plan tailored to specific genetic findings
Early genetic diagnosis opens doors to specialized treatments, supportive therapies, and community resources that can dramatically improve long-term outcomes.
Understanding Your Test Results
We understand that waiting for genetic test results can be stressful. That’s why we provide clear, compassionate guidance throughout the process. Your results will clearly indicate whether POLR1C gene mutations were detected, along with detailed explanations about what this means for your family’s health.
Our genetic counselling team will help you understand the implications of your results and connect you with appropriate medical resources. Whether the results confirm a diagnosis or provide reassuring information, you’ll have the support needed to make the best decisions for your family’s wellbeing.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Turnaround Time |
|---|---|---|---|
| POLR1C Gene Test | ZAR 6,700 | 3-4 Weeks |
This comprehensive testing includes genetic counselling, detailed analysis, and clear result interpretation – providing exceptional value for families seeking definitive answers about Treacher Collins Syndrome.
Why South African Families Trust Oracle Genomics
We’ve built our reputation on accuracy, compassion, and accessibility across South Africa:
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
- Expert Team: Qualified genetic specialists and counsellors guiding you every step
- Advanced Technology: State-of-the-art NGS testing ensuring 99.9% accuracy
- Comprehensive Support: From sample collection to result interpretation and beyond
- Proven Track Record: Thousands of satisfied families across South Africa
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about genetic conditions affect your family’s peace of mind. Our POLR1C gene test provides the answers you need to move forward with confidence.
Sample Collection Options: Blood draw, extracted DNA, or simple blood spot on FTA card
Preparation Required: Clinical history and genetic counselling session to create family pedigree chart
Limited time special pricing – secure your family’s genetic health today. Results typically available within 3-4 weeks.
