Find Answers for Your Child’s Neurological Symptoms with AADC Deficiency Testing
When your child experiences unexplained developmental delays, movement disorders, or neurological symptoms, the uncertainty can be overwhelming. Our AADC deficiency genetic test provides the clarity you need to understand these complex health challenges and create an effective treatment plan.
Understanding AADC Deficiency Genetic Testing
AADC deficiency is a rare genetic disorder that affects the body’s ability to produce essential neurotransmitters like dopamine and serotonin. Our advanced Next-Generation Sequencing (NGS) technology examines the DDC gene to identify mutations that cause this condition. This isn’t just a test – it’s a pathway to understanding your child’s unique neurological needs and accessing targeted treatments that can significantly improve quality of life.
Who Should Consider This Test?
This test is crucial for children and individuals showing:
- Unexplained developmental delays or regression
- Movement disorders including oculogyric crises
- Hypotonia (low muscle tone) and weakness
- Autonomic nervous system dysfunction
- Feeding difficulties and gastrointestinal issues
- Family history of similar neurological conditions
If your child’s symptoms remain unexplained despite multiple evaluations, this genetic test could provide the missing piece to their health puzzle.
Why Early Detection Matters for Your Child’s Health
Receiving an accurate AADC deficiency diagnosis can transform your child’s health journey by:
- Enabling targeted treatment approaches including neurotransmitter precursors
- Preventing unnecessary medical procedures and incorrect treatments
- Providing clarity for educational and developmental planning
- Understanding inheritance patterns for family planning decisions
- Connecting with specialized medical care and support networks
Early intervention can significantly improve neurological outcomes and quality of life.
Understanding Your Test Results
We make understanding your results straightforward and supportive:
- Positive Result: Identifies specific DDC gene mutations – our genetic counsellors will explain what this means for treatment and management
- Negative Result: Rules out AADC deficiency, allowing you to explore other potential causes with your healthcare provider
- Variant of Uncertain Significance: Rare findings that require further evaluation – we provide complete guidance on next steps
Every result includes a comprehensive consultation to ensure you fully understand the implications and next steps.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| Complete AADC Deficiency Genetic Test | ZAR 6,700 |
Your investment includes: NGS genetic analysis, genetic counselling session, comprehensive result interpretation, and ongoing support. Considering the cost of continued specialist visits and misdiagnoses, this test represents significant long-term health savings.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available throughout South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Professional Expertise: Board-certified geneticists and counsellors
- Complete Support: From sample collection to result interpretation
- Rapid Turnaround: Results in 3-4 weeks with ongoing communication
Test Information
- Turnaround Time: 3 to 4 weeks
- Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
- Preparation: Clinical history and genetic counselling session to create family pedigree
- Method: Next-Generation Sequencing (NGS) Technology
- Specialty: General Physician referral recommended
Take the First Step Toward Clarity Today
Don’t let uncertainty about your child’s neurological symptoms continue. Our AADC deficiency test provides the answers you need to move forward with confidence.
Limited time special pricing available. Early detection can make a life-changing difference for your child’s neurological health and development.
