Find Answers for Unexplained Neurological Symptoms
When your child or loved one experiences mysterious neurological symptoms that doctors can’t explain, the uncertainty can be overwhelming. Developmental delays, seizures, or movement disorders without clear cause create anxiety and fear for families across South Africa. Our FOLR1 Gene Neurodegeneration Test provides the clarity you need to understand these complex neurological conditions and take control of your family’s health journey.
Understanding FOLR1 Cerebral Folate Transport Deficiency
FOLR1 gene mutations cause cerebral folate transport deficiency, a rare genetic disorder that prevents folate (vitamin B9) from reaching the brain properly. Without adequate folate, the brain cannot function normally, leading to progressive neurodegeneration. This isn’t just about vitamins – it’s about your brain’s ability to communicate, develop, and maintain healthy function.
Our test uses Next-Generation Sequencing (NGS) technology to examine the FOLR1 gene with exceptional accuracy, identifying even the smallest genetic variations that could be causing neurological symptoms.
Who Should Consider This Genetic Test?
This test is particularly important if you or your child experience:
- Unexplained developmental delays or regression
- Seizures that don’t respond to standard treatments
- Movement disorders or coordination problems
- Progressive neurological decline without clear diagnosis
- Family history of similar neurological conditions
- Autism-like symptoms with neurological components
Many families in Johannesburg, Cape Town, and Durban have found answers through genetic testing when traditional diagnostic methods provided limited results.
Why Early Detection Matters for Your Health
Identifying FOLR1 gene mutations early can be life-changing because:
- Targeted Treatment: Specific treatments like folinic acid supplementation can dramatically improve symptoms
- Prevent Progression: Early intervention may prevent further neurological damage
- Family Planning: Understanding genetic risks helps with informed family decisions
- Peace of Mind: Finally having answers reduces the stress of uncertainty
- Better Outcomes: Early treatment often leads to significantly improved quality of life
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. That’s why we provide:
- Clear Explanations: Results are explained in understandable language
- Genetic Counselling: Included session to help interpret results and discuss implications
- Family Guidance: Information about what results mean for other family members
- Next Steps: Clear recommendations for follow-up care and treatment options
- Ongoing Support: Access to our team for any additional questions
Whether results are positive or negative, you’ll have the information needed to make informed healthcare decisions.
Transparent Pricing & Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| FOLR1 Gene Neurodegeneration Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | Included at no extra cost | ||
| Family Pedigree Analysis | Included in comprehensive service | ||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why Trust Oracle Genomics?
As South Africa’s leading genetic testing provider, we combine medical excellence with compassionate care:
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by specialist neurologists and genetic experts
- Advanced Technology: State-of-the-art NGS technology for maximum accuracy
- Patient-Focused: We understand the emotional journey of genetic testing
- Proven Reliability: Thousands of South Africans trust our genetic testing services
Take the First Step Toward Answers
Don’t let uncertainty about neurological symptoms continue to cause worry and stress. Early detection through genetic testing can provide the answers needed to pursue effective treatment and improve quality of life.
Remember: Early detection of FOLR1 gene mutations can lead to targeted treatments that may significantly improve neurological outcomes. Don’t wait – take control of your family’s neurological health today.
