Understanding Your Genetic Risk for Neurological Conditions
When neurological symptoms appear in your family, the uncertainty can be overwhelming. The ATN1 Gene Dentatorubral-Pallidoluysian Atrophy (DRPLA) test provides the clarity you need to understand your genetic inheritance and plan for your health future with confidence.
What This Test Reveals About Your Health
The ATN1 gene test uses advanced Next-Generation Sequencing (NGS) technology to detect mutations associated with Dentatorubral-pallidoluysian atrophy – a rare, inherited neurological disorder that typically appears in adulthood. This condition affects multiple areas of the brain, leading to progressive movement difficulties, cognitive changes, and coordination challenges.
Our test examines the specific genetic variations in the ATN1 gene that are responsible for DRPLA, providing you with definitive information about your genetic status and potential risk to future generations.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Progressive coordination difficulties or ataxia
- Involuntary muscle movements or chorea
- Cognitive changes or dementia symptoms
- Seizures or epilepsy that developed in adulthood
- Family history of similar neurological symptoms
- Known ATN1 gene mutations in your family lineage
If you’re planning a family and have concerns about genetic inheritance, this test provides crucial information for making informed reproductive decisions.
Why Early Genetic Detection Matters
Understanding your ATN1 gene status empowers you to:
- Receive accurate diagnosis and appropriate medical management
- Access specialised neurological care and support services
- Make informed family planning decisions
- Participate in clinical trials and emerging treatments
- Reduce anxiety through definitive answers
- Connect with support communities and resources
Early detection allows for proactive health management and better quality of life outcomes.
Understanding Your Test Results
Our genetic counsellors provide comprehensive support throughout your testing journey:
- Pre-test counselling: We help document your family history and create a pedigree chart to understand inheritance patterns
- Clear result interpretation: Your results will clearly indicate whether ATN1 gene mutations were detected
- Post-test guidance: We explain what your results mean for your health and family members
- Ongoing support: Connect you with appropriate medical specialists and support resources
Whether your results are positive or negative, you’ll leave with a clear understanding of your genetic status and next steps.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| ATN1 Gene DRPLA NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Includes: Genetic counselling session and comprehensive result interpretation
Why South Africans Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Specialised neurological genetic testing interpreted by qualified professionals
- Advanced Technology: Next-Generation Sequencing ensures highest accuracy standards
- Patient-Centred Care: Empathetic support throughout your genetic testing journey
- Proven Track Record: Trusted by healthcare providers and patients nationwide
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about neurological conditions control your family’s future. Our special ZAR 6,700 pricing makes this crucial genetic testing more accessible than ever.
Limited Time Offer: Special ZAR 6,700 pricing available for immediate bookings. Secure your family’s neurological health future with confidence.
