Find Answers for Unexplained Neurological Symptoms
When your child or loved one experiences developmental delays, muscle weakness, or seizures without clear cause, the uncertainty can be overwhelming. Our POLG Gene Mitochondrial DNA Depletion Syndrome Type 4A test provides the clarity South African families deserve, using cutting-edge NGS technology to uncover genetic answers.
Understanding the POLG Gene Test
The POLG gene plays a crucial role in maintaining your mitochondrial DNA – the energy powerhouses of your cells. When this gene has mutations, it can lead to Mitochondrial DNA Depletion Syndrome Type 4A, a progressive neurological condition that affects energy production throughout the body, particularly in the brain and muscles.
Our Next Generation Sequencing (NGS) technology examines the POLG gene with exceptional accuracy, identifying even subtle genetic changes that might be missed by conventional testing methods.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Unexplained developmental delays in infancy or childhood
- Progressive muscle weakness or loss of motor skills
- Seizures that don’t respond well to standard treatments
- Liver dysfunction alongside neurological symptoms
- Family history of mitochondrial disorders or early childhood neurological conditions
- Multiple unexplained symptoms affecting different body systems
Many South African families spend years searching for answers – our test can provide definitive genetic confirmation in just 3-4 weeks.
Why Early Detection Matters for Your Health
Getting a precise genetic diagnosis offers significant benefits:
- Personalised Treatment Plans: Knowing the specific genetic cause allows doctors to tailor management strategies
- Family Planning Guidance: Understand inheritance patterns for future family decisions
- End Diagnostic Uncertainty: Stop the cycle of endless doctor visits and inconclusive tests
- Access to Specialised Care: Connect with neurologists who understand mitochondrial conditions
- Peace of Mind: Replace anxiety with knowledge and a clear path forward
Understanding Your Test Results
We know waiting for genetic results can be stressful. Our comprehensive report includes:
- Clear explanation of any POLG gene mutations detected
- What the results mean for your health and treatment options
- Guidance on next steps and specialist referrals
- Information about genetic counselling for family members
- Support resources for living with mitochondrial conditions
Our genetic counsellors are available to help you understand your results and make informed healthcare decisions.
Affordable Genetic Testing for South African Families
| Test Feature | Details | Value |
|---|---|---|
| Regular Price | ZAR 9,350 | Comprehensive genetic analysis |
| Special Price | ZAR 6,700 | Save ZAR 2,650 |
| Turnaround Time | 3-4 Weeks | Faster than many international labs |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | Convenient options available |
Consider the cost of ongoing specialist visits, multiple tests, and treatment without clear direction – our test provides answers that can save both money and emotional distress in the long term.
Why Trust Oracle Genomics?
- Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialised neurological genetic testing interpreted by experienced professionals
- Advanced Technology: State-of-the-art NGS methodology for maximum accuracy
- Comprehensive Support: Genetic counselling included to help you understand results and implications
- South African Focus: Understanding local healthcare needs and family dynamics
Take the First Step Toward Answers Today
Don’t let uncertainty about neurological symptoms continue to cause stress and anxiety. With our special pricing of ZAR 6,700, there’s never been a better time to get the genetic answers your family deserves.
Book your test now and receive:
- Genetic counselling session to understand family history
- Convenient sample collection options nationwide
- Comprehensive results explained in clear language
- Support from our team throughout the process
Contact us today to schedule your test or speak with our genetic counselling team. Your journey to answers starts here.
Test Preparation
Before your test, we recommend a genetic counselling session to create a detailed family history pedigree chart. This helps our specialists provide the most accurate interpretation of your results and understand how the condition may affect your family.
