Understanding Your Child’s Movement: PDE10A Gene Dyskinesia Testing
When your baby shows unusual movements or facial expressions, it’s natural to feel concerned and seek answers. The PDE10A Gene Dyskinesia Test provides the clarity you need to understand your child’s neurological health. At Oracle Genomics, we combine cutting-edge NGS technology with compassionate care to deliver reliable results that can guide your family’s healthcare decisions.
What This Test Detects
The PDE10A Gene Dyskinesia Test examines the PDE10A gene for mutations that can cause infantile-onset movement disorders. This specialised test identifies genetic variations that may lead to involuntary movements in limbs and facial muscles, helping you understand the underlying cause of your child’s symptoms.
Using Next-Generation Sequencing (NGS) technology, we provide comprehensive analysis with exceptional accuracy. This advanced approach ensures we don’t miss important genetic information that could impact your child’s treatment and management plan.
Who Should Consider This Test?
This test is particularly important for families where infants show:
- Involuntary limb movements or twitching
- Unusual facial movements or expressions
- Delayed motor development milestones
- Family history of movement disorders
- Unexplained neurological symptoms in infancy
If you’ve noticed your child experiencing movement challenges that concern you, this test can provide the answers needed for proper care and management.
Why Early Detection Matters for Your Child’s Health
Early genetic diagnosis through PDE10A testing offers multiple benefits:
- Personalised Treatment Plans: Accurate diagnosis enables targeted therapies and interventions
- Family Planning Guidance: Understand inheritance patterns for future family decisions
- Reduced Diagnostic Uncertainty: End the cycle of multiple doctor visits and unclear diagnoses
- Improved Quality of Life: Early intervention can significantly enhance developmental outcomes
- Peace of Mind: Knowing the cause reduces anxiety and enables proactive management
Understanding Your Results
We make understanding your genetic results straightforward and supportive:
- Clear Reporting: Results presented in easy-to-understand language with medical guidance
- Genetic Counselling: Professional interpretation and family implications discussion
- Clinical Correlation: How results relate to your child’s specific symptoms
- Next Steps Guidance: Clear recommendations for management and specialist referrals
- Ongoing Support: Access to our team for any follow-up questions
Our genetic counsellors ensure you leave with complete understanding and a clear path forward.
Transparent Pricing – Excellent Value
| Service | Regular Price | Special Price |
|---|---|---|
| PDE10A Gene Dyskinesia NGS Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or Blood on FTA Card
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialist neurologist oversight and genetic counselling
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Patient-Focused Care: Compassionate support throughout your testing journey
- Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Answers
Don’t let uncertainty about your child’s movement development continue. Early detection through genetic testing can provide the clarity needed for proper care and management.
Limited Time Offer: Save ZAR 2,650 on comprehensive PDE10A testing. Book today to secure this special pricing and take control of your child’s neurological health journey.
Early detection leads to better outcomes. Every day matters when it comes to your child’s development and quality of life.
