Find Answers for Unexplained Developmental and Neurological Symptoms
When your child shows concerning symptoms like developmental delays, muscle weakness, or neurological issues without clear cause, the uncertainty can be overwhelming. Our ELAC2 Gene NGS DNA test provides the clarity you need to understand and address Combined Oxidative Phosphorylation Deficiency Type 17 – a serious mitochondrial disorder that affects how your body produces energy.
Understanding the ELAC2 Gene Test
This advanced genetic screening uses Next-Generation Sequencing (NGS) technology to examine the ELAC2 gene, which plays a crucial role in mitochondrial function. Mitochondria are the powerhouses of your cells, and when they don’t work properly due to genetic mutations, it can lead to serious health complications. Our test provides comprehensive analysis with exceptional accuracy, giving you reliable information to guide healthcare decisions.
Who Should Consider This Test?
This test is particularly important if you or your child experience:
- Unexplained developmental delays in infancy or childhood
- Progressive muscle weakness or poor muscle tone
- Neurological symptoms including seizures or movement disorders
- Failure to thrive or growth problems
- Family history of mitochondrial disorders
- Unexplained metabolic issues or lactic acidosis
Early detection through genetic testing can make a significant difference in management and quality of life.
Why Early Detection Matters for Your Health
Identifying Combined Oxidative Phosphorylation Deficiency Type 17 early provides numerous benefits:
- Accurate Diagnosis: Move from uncertainty to clear understanding of symptoms
- Personalised Treatment: Develop targeted management strategies based on genetic findings
- Family Planning: Understand inheritance patterns for future family decisions
- Peace of Mind: Reduce the stress of unknown medical conditions
- Proactive Healthcare: Implement preventive measures and monitoring
Understanding Your Test Results
We make understanding your results straightforward and supportive:
- Clear Reporting: Results presented in easy-to-understand language with medical guidance
- Genetic Counselling: Included session to help interpret results and discuss implications
- Family Pedigree Analysis: Comprehensive family history assessment included
- Ongoing Support: Access to our medical team for questions and next steps
Whether results show a mutation or provide reassurance of normal findings, we’re here to support your healthcare journey.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| ELAC2 Gene NGS DNA Test | ZAR 6,700 | ZAR 2,650 |
What’s Included: Comprehensive genetic analysis, genetic counselling session, family pedigree chart, detailed results report, and ongoing medical support.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified general physicians and genetic specialists
- Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Quick Turnaround: Results typically within 3-4 weeks
- Comprehensive Preparation: Includes clinical history assessment and genetic counselling
Take the First Step Toward Clarity
Don’t let uncertainty about developmental or neurological symptoms continue to worry you. Our ELAC2 Gene test provides the answers you need to move forward with confidence.
Limited Time Special: Save ZAR 2,650 on this comprehensive genetic analysis. Early detection can significantly impact treatment outcomes and quality of life.
Ready for Answers? Contact Oracle Genomics today to schedule your ELAC2 Gene NGS DNA test and take control of your family’s health journey with confidence and clarity.
