Finding Answers for Your Child’s Health Journey
When your child faces complex health challenges, every parent deserves clear answers and compassionate support. The SETBP1 Gene Schinzel-Giedion Midface Retraction Syndrome test provides the diagnostic clarity you need to understand your child’s unique genetic makeup and plan for their future care with confidence.
Understanding the SETBP1 Genetic Test
This advanced genetic test examines the SETBP1 gene using Next-Generation Sequencing (NGS) technology – the gold standard in genetic analysis. The SETBP1 gene plays a crucial role in normal development, and mutations in this gene can lead to Schinzel-Giedion syndrome, a rare condition that affects multiple body systems.
Our test provides comprehensive analysis of the entire SETBP1 gene, identifying even the smallest genetic variations that could impact your child’s health. This level of detail ensures you receive the most accurate diagnostic information available.
Who Should Consider This Genetic Test?
This test is particularly important for families where a child shows:
- Distinctive facial features including midface retraction
- Severe developmental delays or intellectual disability
- Multiple congenital abnormalities
- Seizures or neurological symptoms
- Growth abnormalities or failure to thrive
- Family history of similar conditions
If your paediatrician or genetic specialist has mentioned concerns about Schinzel-Giedion syndrome or related genetic conditions, this test provides the definitive answers you need.
Why Early Genetic Testing Matters for Your Family
Receiving a clear genetic diagnosis can transform your child’s healthcare journey by:
- Providing certainty and ending the diagnostic odyssey
- Enabling targeted medical management and interventions
- Helping predict potential health complications
- Informing family planning decisions
- Connecting you with appropriate support networks
- Reducing unnecessary medical tests and procedures
Early diagnosis means earlier access to specialised care and support services that can significantly improve your child’s quality of life.
Understanding Your Genetic Test Results
Our comprehensive genetic counselling ensures you fully understand your results and their implications. Your report will clearly explain:
- Whether a SETBP1 gene mutation was detected
- The specific type of mutation found
- What this means for your child’s health and development
- Recommended next steps for medical management
- Information about recurrence risks for future pregnancies
Our genetic counsellors are available to discuss your results in detail, answering all your questions with compassion and expertise.
Affordable Genetic Testing for South African Families
| Test Details | Information |
|---|---|
| Regular Price | ZAR 9,350 |
| Special Price | ZAR 6,700 |
| Turnaround Time | 3-4 Weeks |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card |
| Testing Method | Next-Generation Sequencing (NGS) |
This special pricing makes advanced genetic testing accessible to South African families who need answers about complex paediatric conditions.
Why Trust Oracle Genomics?
As South Africa’s leading genetic testing provider, we offer:
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Genetic Counselling: Pre-test counselling to create your family pedigree chart
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Compassionate Care: Understanding the emotional journey of genetic testing
- Quick Results: 3-4 week turnaround for timely decision-making
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s health continue. Our genetic testing provides the clarity you need to make informed healthcare decisions and access appropriate support services.
Book your genetic counselling session now to begin your testing journey. Our team is ready to provide the compassionate, expert care your family deserves.
Contact us today to schedule your appointment or learn more about the SETBP1 genetic testing process. Early detection can make all the difference in your child’s healthcare journey.
