TWIST1 Gene Craniosynostosis Type 1 NGS Genetic DNA Test
As a parent, noticing unusual skull shape or development in your child can be deeply concerning. You want answers, clarity, and the reassurance that comes from understanding what’s happening with your child’s health. Our TWIST1 Craniosynostosis genetic test provides the definitive answers you need to make informed decisions about your child’s care and future.
Understanding Your Child’s Genetic Health
The TWIST1 gene plays a crucial role in skull development during infancy. When mutations occur in this gene, it can lead to craniosynostosis – a condition where the skull bones fuse too early, preventing normal brain growth and causing distinctive facial features. Our advanced NGS (Next Generation Sequencing) technology examines the TWIST1 gene with exceptional precision, identifying even the smallest genetic variations that could impact your child’s development.
Is This Test Right for Your Child?
This test is specifically designed for families who notice:
- Unusual skull shape or premature fusion of skull bones
- Family history of craniosynostosis or Saethre-Chotzen syndrome
- Distinctive facial features like drooping eyelids or low-set ears
- Developmental delays that might be linked to skull development issues
- Previous concerns raised by paediatricians about head shape
Early detection can make a significant difference in managing potential complications and planning appropriate interventions.
Why Early Detection Matters for Your Child’s Future
Getting this test provides crucial benefits:
- Peace of Mind: Eliminate uncertainty about your child’s condition
- Early Intervention: Plan appropriate medical care before complications develop
- Family Planning: Understand inheritance patterns for future children
- Prevent Complications: Reduce risk of increased intracranial pressure and vision problems
- Personalised Care: Work with specialists to create the best treatment plan
Understanding Your Results with Confidence
We know waiting for genetic test results can be anxiety-provoking. That’s why we provide:
- Clear, Comprehensive Reports: Easy-to-understand results with detailed explanations
- Genetic Counselling: Professional guidance to help you understand what the results mean for your family
- Medical Referrals: Connections to specialists who can help with next steps
- Ongoing Support: Our team remains available to answer your questions
Whether the results confirm a diagnosis or provide reassuring news, you’ll have the information and support needed to move forward confidently.
Affordable, Accessible Genetic Testing
| Test Option | Price | Turnaround Time |
|---|---|---|
| Special Price | ZAR 6,700 | 3-4 Weeks |
| Regular Price | ZAR 9,350 | 3-4 Weeks |
Price includes comprehensive genetic counselling and detailed result interpretation
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- 99.9% Accuracy: Advanced NGS technology ensures reliable results
- Expert Team: Genetic specialists with years of paediatric experience
- Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
- Complete Preparation Support: We help gather clinical history and create family pedigree charts
Take the First Step Toward Clarity Today
Don’t let uncertainty about your child’s health create unnecessary stress. With our special pricing of ZAR 6,700, comprehensive genetic counselling, and nationwide availability, there’s no reason to delay getting the answers your family deserves.
Limited Time Offer: Special pricing of ZAR 6,700 available for a limited time only. Regular price ZAR 9,350.
Convenient Locations: Testing available throughout South Africa including Johannesburg, Cape Town, Durban, and Pretoria.
