Find Clarity and Peace of Mind with 4H Syndrome Genetic Testing
When neurological symptoms appear in your child, the uncertainty can be overwhelming. The Nx Gen Sequencing 4H Syndrome Test provides the answers South African families need to understand rare genetic conditions and plan for the future with confidence.
Understanding 4H Syndrome Genetic Testing
4H Syndrome (Hypomyelination, Hypodontia, Hypogonadotropic Hypogonadism) is a rare neurological disorder that affects brain development, dental formation, and hormonal regulation. Our advanced Nx Gen sequencing technology examines the POLR3A and POLR3B genes to identify mutations that cause this condition, providing families with definitive answers and a clear path forward.
Who Should Consider This Test?
This test is recommended for individuals showing symptoms such as:
- Delayed motor development and coordination difficulties
- Progressive neurological symptoms including ataxiaDental abnormalities or missing teeth
- Growth and puberty delays
- Family history of similar neurological conditions
If your child is experiencing these symptoms, early genetic testing can provide crucial information for proper medical management.
Why Early Detection Matters for Your Family’s Health
Getting a definitive diagnosis through genetic testing offers numerous benefits:
- Accurate Diagnosis: Eliminate uncertainty and get clear answers about your child’s condition
- Personalised Treatment: Enable healthcare providers to create targeted management plans
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Access appropriate therapies and support services sooner
- Peace of Mind: Reduce anxiety by understanding the condition and its progression
Understanding Your Test Results
Our genetic counsellors and medical specialists will help you understand your results in clear, compassionate terms. We provide:
- Detailed explanation of genetic findings
- Guidance on next steps and medical management
- Referrals to appropriate specialists if needed
- Ongoing support for your family’s journey
Remember, genetic information empowers you to make informed healthcare decisions for your loved ones.
Affordable Genetic Testing for South African Families
| Test Option | Price | Savings |
|---|---|---|
| Special Price | ZAR 7,800 | ZAR 900 off regular price |
| Regular Price | ZAR 8,700 | – |
This comprehensive genetic analysis represents excellent value compared to international testing options, making advanced diagnostics accessible to South African families.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests reviewed by qualified neurologists and genetic specialists
- Advanced Technology: Cutting-edge NGS and Sanger sequencing for maximum accuracy
- Fast Turnaround: Samples processed daily by 9 am, results in 40 working days
- Patient Privacy: Strict confidentiality and ethical testing practices
Test Requirements
Sample Type: 10 mL (5 mL minimum) whole blood from 2 Lavender Top (EDTA) tubes
Important: Ship refrigerated. DO NOT FREEZE. Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Specialties: Neurologist, Dentist, Pediatrician
Take the First Step Toward Answers Today
Don’t let uncertainty about neurological symptoms continue to worry your family. Our compassionate team is ready to help you get the clarity you deserve.
Limited Time Offer: Save ZAR 900 on comprehensive 4H Syndrome genetic testing. Book your appointment today and take control of your family’s health journey.
