Find Clarity About Lesch-Nyhan Syndrome Genetic Risks
When neurological symptoms appear or family history raises concerns, uncertainty can feel overwhelming. Our HPRT1 gene test provides the definitive answers you need to understand your genetic risk for Lesch-Nyhan syndrome – a rare but serious neurological disorder that affects movement and behaviour.
Many South African families wait too long for answers, delaying crucial management strategies. With our advanced genetic testing, you can move from uncertainty to understanding in just 3-4 weeks.
Understanding the HPRT1 Gene Test
The HPRT1 gene test examines your DNA for mutations in the hypoxanthine phosphoribosyltransferase 1 gene. When this gene doesn’t function properly, it leads to Lesch-Nyhan syndrome – a condition that affects the nervous system and causes movement disorders, cognitive challenges, and behavioural issues.
Using Next Generation Sequencing (NGS) technology, we analyse your genetic code with exceptional precision. This isn’t just a screening test; it’s a comprehensive diagnostic tool that provides clear, actionable results.
Who Should Consider This Test?
This test is particularly important if you or your child experience:
- Involuntary muscle movements or dystonia
- Developmental delays in motor skills
- Self-injurious behaviours
- Family history of neurological disorders
- Unexplained gout or kidney stones in childhood
- Abnormal uric acid levels
Many patients from Johannesburg to Cape Town find that early genetic testing provides the clarity needed to pursue appropriate treatments and management strategies.
Why Early Detection Matters for Your Health
Knowing your genetic status empowers you to:
- Access targeted treatments and therapies earlier
- Implement preventive measures for symptom management
- Make informed family planning decisions
- Reduce anxiety through definitive diagnosis
- Connect with appropriate specialists and support networks
Early intervention can significantly improve quality of life and help manage the neurological symptoms associated with Lesch-Nyhan syndrome.
Understanding Your Test Results
We make understanding your results straightforward and reassuring:
- Positive Result: Indicates a mutation in the HPRT1 gene. Our genetic counsellors will explain what this means for you and connect you with appropriate neurological specialists.
- Negative Result: No mutation detected, providing peace of mind about your genetic risk.
- Uncertain Variant: Rare cases where significance is unclear – we provide ongoing monitoring and interpretation.
Every result comes with professional genetic counselling to ensure you fully understand the implications and next steps.
Transparent Pricing – Exceptional Value
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| HPRT1 Gene Lesch-Nyhan Syndrome Test | ZAR 6,700 | ZAR 2,650 |
Includes genetic counselling session and comprehensive result interpretation
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: Using cutting-edge NGS sequencing for maximum accuracy
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Genetic Counselling: Professional guidance throughout your testing journey
- Quick Turnaround: Results typically within 3-4 weeks
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about neurological symptoms control your life. Our HPRT1 gene test provides the answers you need to make informed health decisions.
Limited Time Offer: Save ZAR 2,650 on this comprehensive genetic analysis. Book your test today and receive:
- Professional genetic counselling session
- Family pedigree analysis
- Comprehensive result interpretation
- Connection to neurological specialists if needed
Contact us today to schedule your test at one of our nationwide locations or through our convenient mobile collection service.
