Finding Answers for Your Child’s Movement Concerns
When your infant shows unusual movements, muscle stiffness, or developmental delays, it’s natural to feel concerned and seek clear answers. Our SLC6A3 Gene Parkinsonism-Dystonia test provides the clarity you need to understand your child’s health journey.
As parents, you deserve accurate information and compassionate support. This specialised genetic test helps identify the underlying causes of movement disorders in infants, giving you the knowledge to make informed decisions about your child’s care.
Understanding the SLC6A3 Gene Test
The SLC6A3 gene plays a crucial role in dopamine transport in the brain. When mutations occur in this gene, it can lead to infantile Parkinsonism-Dystonia – a condition affecting movement control and muscle coordination.
Our test uses Next Generation Sequencing (NGS) technology, the most advanced method available, to examine the SLC6A3 gene for any abnormalities. This comprehensive analysis provides detailed information about potential genetic causes of your child’s symptoms.
Who Should Consider This Test?
This test is recommended for infants showing:
- Unusual muscle stiffness or rigidity
- Tremors or involuntary movements
- Developmental delays in motor skills
- Difficulty with coordination and balance
- Family history of movement disorders
- Progressive worsening of movement symptoms
If your child is experiencing any of these symptoms, early genetic testing can provide valuable insights for their healthcare team.
Why Early Diagnosis Matters for Your Child’s Health
Getting an accurate diagnosis early can significantly impact your child’s development and quality of life. Benefits include:
- Targeted Treatment Planning: Knowing the specific genetic cause helps doctors create personalised treatment strategies
- Early Intervention: Begin appropriate therapies and interventions sooner
- Family Planning Insights: Understand inheritance patterns for future family planning
- Peace of Mind: Reduce uncertainty and anxiety about your child’s condition
- Better Management: Work with specialists to manage symptoms effectively
Understanding Your Test Results
We understand that waiting for genetic test results can be stressful. Our process is designed to be as clear and supportive as possible:
Turnaround Time: 3-4 weeks from sample receipt
Sample Collection: Simple blood draw or FTA card sample (just one drop of blood)
Comprehensive Support: Includes genetic counselling to help interpret results and understand family implications
Your results will be explained in clear, understandable language, and our genetic counsellors are available to answer any questions you may have.
Affordable, Accessible Genetic Testing
| Test Option | Price | Savings |
|---|---|---|
| Special Price | ZAR 6,700 | ZAR 2,650 off |
| Regular Price | ZAR 9,350 | – |
This investment in your child’s health provides lifelong benefits through accurate diagnosis and proper management.
Why Trust Oracle Genomics?
Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
Specialist Expertise: Tests performed and interpreted by qualified neurologists
Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
Comprehensive Support: Genetic counselling included to support your family’s journey
Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Understanding Your Child’s Health
Don’t wait to get the answers you need. Early diagnosis can make a significant difference in your child’s development and quality of life.
Book Your Test Today: Contact us to schedule your genetic counselling session and testing appointment. Our compassionate team is ready to support you through this important health journey.
Limited time special pricing available – secure your child’s health future now.
