Find Answers for Mitochondrial Phosphate Carrier Deficiency
When your child shows unexplained muscle weakness, developmental delays, or metabolic symptoms, the uncertainty can be overwhelming. Our SLC25A3 gene test provides the clarity you need to move forward with confidence and create the best possible care plan for your loved one.
Understanding Your Genetic Health
The SLC25A3 gene plays a crucial role in your body’s energy production system. When this gene isn’t working properly, it can lead to mitochondrial phosphate carrier deficiency – a condition that affects how your cells generate energy. Our advanced NGS (Next Generation Sequencing) technology examines this specific gene with exceptional accuracy, giving you definitive answers about your genetic health.
Who Should Consider This Important Test?
This test is particularly important if you or your child experience:
- Unexplained muscle weakness or fatigue
- Developmental delays in childhood
- Metabolic disorders or energy production issues
- Family history of mitochondrial conditions
- Unexplained neurological symptoms
- Growth concerns in infants and children
Many South African families have found life-changing answers through this testing, enabling them to pursue targeted treatments and management strategies.
Why Early Detection Matters for Your Family
Getting clear genetic answers provides multiple benefits:
- Peace of Mind: End the uncertainty and know exactly what you’re dealing with
- Targeted Treatment: Work with your healthcare team to develop specific management plans
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Start appropriate therapies and support sooner for better outcomes
- Reduced Medical Costs: Avoid unnecessary tests and treatments by having clear genetic information
Understanding Your Results with Compassion
We know waiting for genetic results can be stressful. Our team provides:
- Clear, easy-to-understand result explanations
- Genetic counselling support to help you understand the implications
- Guidance on next steps and available resources
- Connection to specialist healthcare providers if needed
- Ongoing support for your family’s journey
Your results will be delivered within 3-4 weeks, and our genetic counsellors are available to help you understand what they mean for your family.
Affordable Genetic Testing for South African Families
| Test Description | Regular Price | Special Price |
|---|---|---|
| SLC25A3 Gene Mitochondrial Phosphate Carrier Deficiency NGS Test | R6,700 |
This comprehensive testing represents excellent value compared to the cost of ongoing uncertainty and multiple specialist consultations.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Working with general physicians and genetic specialists
- Advanced Technology: Using cutting-edge NGS sequencing for 99.9% accuracy
- Patient-Focused: We understand the emotional journey of genetic testing
- Confidential Service: Your privacy and data security are our top priorities
Take the First Step Toward Clarity Today
Don’t let uncertainty about mitochondrial conditions delay your family’s health journey. Our compassionate team is ready to support you through this important testing process.
Limited Time Special: Book your SLC25A3 gene test now and save R2,650 off the regular price. Early detection could make all the difference for your family’s health future.
Ready for Answers? Contact Oracle Genomics today and take control of your genetic health journey. Our team is here to provide the clarity and support your family deserves.
Test Specifications:
- Turnaround Time: 3-4 weeks
- Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
- Preparation Required: Clinical history and genetic counselling session
- Technology: Next Generation Sequencing (NGS)
- Specialty: General Physician with Genetic Support
