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OPHN1 Gene X-Linked Mental Retardation with Cerebellar Hypoplasia NGS Genetic Test

Original price was: R9,350.Current price is: R6,700.

-28%

Facing concerns about X-linked mental retardation in your family? Our OPHN1 gene test provides definitive answers about this inherited condition affecting brain development. For just ZAR 6,700 (regularly ZAR 9,350), you’ll receive comprehensive genetic screening using advanced NGS technology. This test specifically identifies mutations in the OPHN1 gene, which causes X-linked mental retardation with cerebellar hypoplasia and distinctive facial features. Early detection empowers families with crucial information for better management and informed family planning decisions. Our testing process includes genetic counselling to understand your family history and provide personalised guidance. With results in 3-4 weeks and nationwide coverage across South Africa, we make genetic testing accessible and trustworthy. Take control of your family’s genetic health journey with confidence and clarity.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
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OPHN1 Gene Test R6
OPHN1 Gene X-Linked Mental Retardation with Cerebellar Hypoplasia NGS Genetic Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding OPHN1 Gene X-Linked Mental Retardation: Your Path to Clarity

When developmental concerns affect your family, the uncertainty can be overwhelming. Our OPHN1 gene test provides the answers you need to understand X-linked mental retardation with cerebellar hypoplasia – a condition that affects brain development and can impact multiple generations. We understand the emotional weight of genetic testing, which is why we’ve created a supportive, confidential process that puts your family’s wellbeing first.

What This Test Reveals About Your Genetic Health

The OPHN1 gene test uses Next Generation Sequencing (NGS) technology to identify mutations in the OPHN1 gene, which is responsible for X-linked mental retardation. This condition primarily affects males and is characterised by:

  • Intellectual disability and developmental delays
  • Cerebellar hypoplasia (underdeveloped cerebellum affecting coordination)
  • Distinctive facial features that may become apparent over time
  • Potential speech and motor skill challenges

By detecting these genetic changes early, families can better understand the condition’s inheritance pattern and make informed decisions about care and management.

Is This Test Right for Your Family?

Consider OPHN1 gene testing if your family experiences:

  • Multiple male relatives with intellectual disability or developmental delays
  • Family history suggesting X-linked inheritance patterns
  • Children showing coordination difficulties or distinctive facial features
  • Unexplained developmental concerns in male family members
  • Planning for future pregnancies with family history of mental retardation

Early identification can transform uncertainty into actionable knowledge, helping you provide the right support at the right time.

Why Early Detection Matters for Your Family’s Future

Getting tested provides more than just answers – it offers peace of mind and practical benefits:

  • Informed Family Planning: Understand inheritance risks for future generations
  • Early Intervention: Access appropriate therapies and support services sooner
  • Reduced Diagnostic Uncertainty: End the cycle of unanswered questions
  • Personalised Care Planning: Tailor educational and therapeutic approaches
  • Emotional Closure: Replace worry with understanding and acceptance

Understanding Your Results with Compassion

We know waiting for genetic results can be stressful. That’s why we provide:

  • Clear, Understandable Reports: Written in plain language with medical guidance
  • Genetic Counselling Support: Professional interpretation of what your results mean
  • Family Implications: Guidance on how results affect other family members
  • Next Steps Planning: Practical recommendations based on your specific situation
  • Ongoing Support: Access to resources and specialist referrals as needed

Our team ensures you never feel alone in understanding your genetic information.

Affordable Genetic Testing with Exceptional Value

Service Regular Price Special Price Savings
OPHN1 Gene NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes: Comprehensive genetic analysis, genetic counselling session, detailed results interpretation, and ongoing support access.

Turnaround Time: 3-4 weeks from sample receipt

Sample Options: Blood, extracted DNA, or blood spot on FTA card

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing across Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
  • Patient-Centred Care: We understand the emotional aspects of genetic testing
  • Proven Reliability: Trusted by healthcare professionals and families nationwide

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about genetic conditions cloud your family’s future. With our special pricing of ZAR 6,700, comprehensive genetic testing is more accessible than ever.

Ready to begin? Contact us today to schedule your genetic counselling session and testing. Our compassionate team is here to guide you through every step of this important journey.

Limited time special pricing – secure your family’s genetic health information while this offer lasts.