Understanding Your Child’s Development: ANKRD11 Gene KBG Syndrome Testing
As a parent, watching your child grow and develop brings both joy and concern. When developmental milestones aren’t met as expected, or when you notice unique facial features and learning challenges, it’s natural to seek answers. Our ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test provides the clarity and understanding you need to support your child’s health journey with confidence and compassion.
What This Test Reveals About Your Child’s Health
The ANKRD11 gene plays a crucial role in normal development, and mutations in this gene can lead to KBG syndrome – a condition characterised by distinctive facial features, developmental delays, and learning challenges. Our advanced Next-Generation Sequencing (NGS) technology examines this specific gene with exceptional accuracy, helping identify whether KBG syndrome is affecting your child’s development.
Unlike basic genetic tests, our comprehensive analysis provides detailed information about specific mutations, giving you and your healthcare provider the precise information needed to create an effective care plan.
Is This Test Right for Your Child?
Many South African families find answers through this test when they notice:
- Unexplained developmental delays in speech, motor skills, or social interaction
- Distinctive facial features including widely spaced teeth, prominent ears, or a triangular face shape
- Learning difficulties or intellectual disability concerns
- Short stature compared to peers
- Behavioural challenges or attention difficulties
- Family history of similar developmental patterns
If you’ve been searching for answers about your child’s unique development pattern, this test can provide the clarity that transforms uncertainty into actionable understanding.
Why Early Detection Matters for Your Family
Getting answers through genetic testing brings multiple benefits that extend beyond diagnosis:
- Personalised Support: Understand your child’s specific needs to access targeted therapies and educational support
- Family Planning: Make informed decisions about future family planning with genetic counselling guidance
- Reduced Anxiety: Replace uncertainty with clear understanding and a defined path forward
- Early Intervention: Access appropriate interventions during critical developmental windows
- Medical Management: Work with healthcare providers to address associated health concerns proactively
Many families report that receiving a clear diagnosis brings relief and direction after years of searching for answers.
Understanding Your Results with Compassion
We understand that waiting for genetic test results can be an anxious time. Our process is designed to provide clarity and support:
- Clear Reporting: Results are presented in easy-to-understand language with medical interpretation
- Genetic Counselling: Included session helps you understand what the results mean for your family
- Family Pedigree: We create a detailed family history chart to understand inheritance patterns
- Next Steps Guidance: Practical recommendations for medical follow-up and support services
- Ongoing Support: Access to resources and information to help you navigate your child’s healthcare journey
Whether the results confirm KBG syndrome or provide alternative explanations, you’ll have the information needed to move forward with confidence.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| ANKRD11 Gene KBG Syndrome NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED | ||
| Family Pedigree Analysis | INCLUDED | ||
| Results Interpretation | INCLUDED | ||
This comprehensive package represents exceptional value compared to pursuing these services separately through multiple providers.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Advanced Technology: Next-Generation Sequencing provides superior accuracy over traditional methods
- Expert Team: Genetic specialists with experience in paediatric developmental conditions
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card for convenience
- Proven Track Record: Trusted by healthcare providers and families throughout South Africa
- Clear Timeline: Results typically available within 3-4 weeks
Take the First Step Toward Understanding
Don’t let uncertainty about your child’s development create unnecessary stress. Early detection through genetic testing can provide the answers that lead to better support and improved outcomes.
Limited Time Special: Book your ANKRD11 Gene KBG Syndrome test at the special price of ZAR 6,700 – saving you ZAR 2,650 off the regular price.
Take action today – understanding your child’s genetic makeup is the first step toward providing the targeted support they need to thrive.
