Find Answers for Unexplained Neurological and Liver Symptoms
When movement disorders, liver complications, or blood abnormalities appear without clear cause, it can be frightening and isolating. Our SLC30A10 genetic test provides the clarity you need to understand rare genetic conditions affecting manganese metabolism. We understand the anxiety that comes with unexplained symptoms, and we’re here to provide accurate answers and a clear path forward.
Understanding the SLC30A10 Genetic Test
This advanced genetic test examines the SLC30A10 gene using Next-Generation Sequencing technology to identify mutations that disrupt manganese transport in your body. When this gene doesn’t function properly, manganese accumulates to toxic levels, leading to a complex condition called hypermanganesemia with dystonia, polycythemia, and cirrhosis.
Think of it as finding the root cause of multiple health issues that may seem unrelated – from movement problems to liver damage and blood abnormalities. Our test provides the genetic evidence needed for accurate diagnosis and targeted treatment.
Who Should Consider This Test?
This test is essential if you or family members experience:
- Unexplained movement disorders or dystonia (involuntary muscle contractions)
- Liver function abnormalities or early signs of cirrhosis
- Polycythemia (elevated red blood cell count)
- Neurological symptoms that began in childhood or adolescence
- Family history of similar neurological or liver conditions
- Multiple family members with movement disorders or liver disease
If you’ve been searching for answers across different specialists without success, this genetic test could provide the missing piece to your health puzzle.
Why Early Detection Matters for Your Health
Identifying SLC30A10 gene mutations early can transform your health journey:
- Prevent irreversible damage – Early intervention can stop neurological progression
- Targeted treatment – Specific therapies can manage manganese levels effectively
- Family planning insights – Understand inheritance patterns for future generations
- End diagnostic uncertainty – Move from confusion to clear action steps
- Peace of mind – Replace anxiety with understanding and control
Many patients experience relief simply from having a definitive answer after years of uncertainty.
Understanding Your Results with Compassion
We know waiting for genetic results can be stressful. Our process is designed to support you every step of the way:
- Genetic counselling session before testing to understand your family history
- Clear, comprehensive report explaining your results in understandable language
- Follow-up consultation to discuss results and next steps
- Connection to specialists who understand this rare condition
- Ongoing support for you and your family throughout the process
Whether your results confirm a diagnosis or provide reassurance, we’ll help you understand what they mean for your health journey.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| SLC30A10 Genetic Test | R6,700 | R2,650 |
Your investment includes: Comprehensive genetic analysis, genetic counselling session, detailed results report, and follow-up consultation. Compare this to months or years of specialist visits without answers.
Why Trust Oracle Genomics?
- Nationwide Coverage – Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Genetic Team – Specialists in rare genetic disorders
- Advanced NGS Technology – Most accurate genetic testing available
- 3-4 Week Turnaround – Faster than many international labs
- Multiple Sample Options – Blood, extracted DNA, or simple FTA card
- Complete Confidentiality – Your privacy is our priority
Take Control of Your Health Journey Today
Don’t let uncertainty about neurological or liver symptoms continue to impact your quality of life. Early detection through genetic testing can provide the answers you need to move forward with confidence.
Book your genetic counselling session now and take the first step toward clarity. Our team is ready to support you through this important health decision.
Limited time special pricing available. Don’t delay getting the answers that could transform your health outlook.
