Understanding SAMHD1 Gene Testing: Your Path to Clarity About Rare Neurological Conditions
When neurological symptoms appear in your child or family members, the uncertainty can be overwhelming. Our SAMHD1 Gene Aicardi-Goutieres Syndrome Type 5 NGS Genetic DNA Test provides the answers you need with compassion and clinical excellence. This advanced genetic screening helps identify mutations that cause this rare brain disorder, giving you the clarity to make informed healthcare decisions for your family’s future.
What This Test Detects
The SAMHD1 gene test uses cutting-edge Next Generation Sequencing (NGS) technology to examine your DNA for specific mutations linked to Aicardi-Goutieres Syndrome Type 5. This rare neurological condition affects brain development and can cause progressive symptoms that often appear in infancy. By identifying these genetic changes early, we can help guide appropriate medical management and provide valuable information for your entire family.
Who Should Consider This Test
This test is particularly important if your child or family members experience:
- Unexplained neurological symptoms appearing in infancy
- Developmental delays or regression
- Microcephaly (small head size)
- Seizures or abnormal movements
- Family history of similar neurological conditions
- Unexplained brain calcifications or white matter changes
Early genetic testing can provide crucial answers when symptoms suggest a possible inherited neurological disorder.
Why Early Detection Matters for Your Family’s Health
Getting definitive answers through genetic testing provides multiple benefits:
- Peace of Mind: Reduce uncertainty about your child’s condition
- Treatment Guidance: Help healthcare providers develop appropriate care plans
- Family Planning: Understand inheritance patterns for future pregnancies
- Early Intervention: Access appropriate therapies and support services sooner
- Medical Management: Guide ongoing neurological care and monitoring
Understanding Your Test Results
Our comprehensive genetic counselling ensures you fully understand your results. We provide:
- Clear explanation of genetic findings in plain language
- Discussion of what results mean for your child’s health
- Guidance on next steps and available support resources
- Family pedigree analysis to understand inheritance patterns
- Connection to appropriate medical specialists if needed
Our team supports you through every step, ensuring you never feel alone in this journey.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| SAMHD1 Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing from Johannesburg to Cape Town, Durban to Pretoria
- Medical Expertise: Specialist neurologist-reviewed testing protocols
- Advanced Technology: State-of-the-art NGS genetic sequencing
- Comprehensive Support: Genetic counselling included with every test
- Patient-Focused Care: Empathetic support throughout your testing journey
Take the First Step Toward Answers Today
Don’t let uncertainty about neurological symptoms continue to worry you. Our SAMHD1 gene test provides the clarity you need to make informed decisions about your family’s health.
Book your genetic counselling session now and take control of your family’s neurological health journey.
Available nationwide across South Africa – from major cities to regional centres.
