Understanding Your Child’s Genetic Health: GLI3 Gene Testing for Greig Syndrome
As a parent, noticing unusual physical features in your child can be worrying. When extra fingers or toes, abnormal head shape, or syndactyly (webbed fingers) appear, it’s natural to seek answers. Our GLI3 Gene Greig Cephalopolysyndactyly Syndrome NGS Genetic DNA Test provides the clarity and certainty you need to make informed healthcare decisions for your child’s future.
What This Test Detects
This advanced genetic test specifically analyses the GLI3 gene using Next-Generation Sequencing (NGS) technology to identify mutations that cause Greig cephalopolysyndactyly syndrome. This rare genetic condition affects bone development, particularly in the skull, hands, and feet. Our test provides definitive genetic confirmation, eliminating uncertainty and guiding appropriate medical management.
Who Should Consider This Test?
This test is recommended if your child shows any of these symptoms:
- Extra fingers or toes (polydactyly)
- Fused or webbed fingers/toes (syndactyly)
- Unusual head shape or prominent forehead
- Widely spaced eyes (hypertelorism)
- Family history of similar physical features
- Developmental delays associated with cranial abnormalities
Early genetic testing can provide crucial information for treatment planning and developmental support.
Why Early Detection Matters for Your Child’s Health
Getting a definitive genetic diagnosis offers multiple benefits:
- Peace of Mind: End the uncertainty about your child’s condition
- Personalised Care: Guide appropriate medical interventions and surgeries
- Family Planning: Understand inheritance patterns for future pregnancies
- Early Intervention: Access developmental support services sooner
- Reduced Anxiety: Replace worry with a clear action plan
Understanding Your Results
We make genetic testing results easy to understand. Your comprehensive report will clearly indicate:
- Presence or absence of GLI3 gene mutations
- Specific genetic changes identified
- What the results mean for your child’s health
- Recommended next steps and specialists to consult
Our included genetic counselling session ensures you fully understand the implications and can make informed decisions about your child’s care.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| GLI3 Gene Greig Syndrome NGS Test | R9,350 | R6,700 | R2,650 |
What’s Included: Comprehensive genetic analysis, professional genetic counselling session, detailed results report, and ongoing support.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Expert Team: Qualified genetic counsellors and medical professionals
- Fast Results: 3-4 week turnaround time
- Multiple Sample Options: Blood, extracted DNA, or blood spot on FTA card
Take Action for Your Child’s Health Today
Don’t let uncertainty about your child’s development cause unnecessary stress. Our trusted genetic testing service provides the answers you need to move forward with confidence.
Limited Time Offer: Save R2,650 on this comprehensive genetic test. Early detection can make a significant difference in your child’s developmental outcomes.
“The peace of mind we gained from getting a definitive diagnosis helped us focus on the right treatments for our daughter. The genetic counselling was incredibly helpful.” – Satisfied Parent, Johannesburg
Nationwide Accessibility
We serve patients across South Africa with testing centres in major cities and sample collection facilities nationwide. Distance is no barrier to getting the genetic answers your family needs.
