Finding Answers for Your Child’s Developmental Journey
When your child faces developmental challenges or neurological symptoms, the uncertainty can be overwhelming. Many South African parents worry about unexplained delays, speech difficulties, or movement disorders. Our UBE3A Gene Angelman Syndrome NGS Genetic DNA Test provides the clarity you need to move forward with confidence and create the best possible care plan for your child’s unique needs.
Understanding Angelman Syndrome Genetic Testing
Angelman Syndrome is a complex genetic condition that affects neurological development. Our advanced NGS (Next Generation Sequencing) technology examines the UBE3A gene with precision, identifying genetic variations that may cause this condition. This isn’t just a test – it’s a comprehensive diagnostic tool that provides definitive answers about your child’s genetic makeup, helping you understand the underlying causes of developmental concerns.
Is This Test Right for Your Family?
Consider this genetic test if your child shows:
- Significant developmental delays or intellectual disability
- Speech impairment or absence of speech
- Movement or balance disorders (ataxia)
- Frequent laughter or smiling that seems inappropriate
- Seizures or epilepsy symptoms
- Sleep disturbances or unusual sleep-wake cycles
- Family history of similar neurological conditions
Many South African families find that early genetic testing provides the foundation for targeted interventions and specialised care plans.
Why Early Detection Matters for Your Child’s Future
Getting a definitive diagnosis through genetic testing offers numerous benefits:
- Personalised Care Planning: Understand your child’s specific needs to create effective intervention strategies
- Reduced Diagnostic Uncertainty: End the cycle of multiple doctor visits and unclear diagnoses
- Family Planning Guidance: Understand genetic risks for future pregnancies
- Access to Specialised Support: Connect with appropriate therapies and educational resources
- Peace of Mind: Replace uncertainty with clear understanding and actionable information
Understanding Your Results with Professional Support
Your journey doesn’t end with the test – it begins with understanding. We provide comprehensive genetic counselling to help you interpret results and plan next steps. Our team explains findings in clear, compassionate language and connects you with appropriate healthcare resources. You’ll receive:
- Clear, detailed report explaining genetic findings
- Professional genetic counselling session
- Guidance on next steps and available support
- Referrals to specialist healthcare providers if needed
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| UBE3A Gene Angelman Syndrome NGS Test | ZAR 6,700 | ZAR 2,650 | |
| Genetic Counselling Session | INCLUDED | ||
| Nationwide Sample Collection | INCLUDED | ||
Turnaround time: 3-4 weeks | Sample type: Blood, Extracted DNA, or Blood on FTA Card
Why South African Families Trust Oracle Genomics
Nationwide Accessibility
Convenient testing available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
Medical Expertise
Specialised neurological genetic testing supervised by experienced professionals
Advanced Technology
State-of-the-art NGS technology ensuring accurate, reliable results
Complete Confidentiality
Your privacy and genetic information are protected with strict security measures
Take the First Step Toward Clarity Today
Don’t let uncertainty about your child’s development create unnecessary stress. Our genetic testing provides the answers you need to make informed healthcare decisions. With convenient locations across South Africa and comprehensive support throughout the process, getting tested has never been easier.
Limited Time Offer: Save ZAR 2,650 on this comprehensive genetic testing package. Early detection can make a significant difference in your child’s developmental journey.
