Sale!

FGFRL1 Gene Radioulnar Synostosis NGS Genetic DNA Test

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

-28%

If you or your child experiences limited elbow movement, forearm stiffness, or has a family history of bone fusion conditions, our FGFRL1 Gene Radioulnar Synostosis DNA Test provides the answers you need. This comprehensive NGS genetic test accurately detects mutations in the FGFRL1 gene that cause radioulnar synostosis – a condition where the forearm bones fuse together. For only ZAR 6,700 (regularly ZAR 9,350), you’ll receive precise genetic insights that can guide treatment decisions and help manage symptoms effectively. Our test is conducted using advanced Next Generation Sequencing technology, ensuring the highest accuracy and reliability. With genetic counselling included, you’ll understand your results clearly and receive professional guidance. Available nationwide across South Africa, including Johannesburg, Cape Town, and Durban, this test offers peace of mind and empowers you to take control of your bone health.

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

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

FGFRL1 Gene Radioulnar Synostosis DNA Test | ZAR 6
FGFRL1 Gene Radioulnar Synostosis NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

Find Clarity About Your Forearm Health with FGFRL1 Genetic Testing

Living with limited elbow movement or forearm stiffness can be frustrating and concerning, especially when you don’t know the cause. If you’ve noticed restricted arm rotation or have a family history of bone fusion conditions, our FGFRL1 Gene Radioulnar Synostosis DNA Test provides the answers you deserve. This advanced genetic test helps identify the underlying genetic factors affecting your bone development, giving you the clarity needed to make informed health decisions.

Understanding Your FGFRL1 Genetic Test

The FGFRL1 gene plays a crucial role in bone development and growth. When mutations occur in this gene, it can lead to radioulnar synostosis – a condition where the radius and ulna bones in your forearm fuse together, limiting rotation and movement. Our test uses Next Generation Sequencing (NGS) technology to examine your FGFRL1 gene with exceptional precision, identifying even the smallest genetic variations that could be affecting your bone health.

This isn’t just another genetic test – it’s a comprehensive analysis that provides specific, actionable information about your condition. By understanding your genetic makeup, you and your healthcare provider can develop targeted strategies to manage symptoms and improve your quality of life.

Who Should Consider This Genetic Test?

This test is particularly important if you or your child experience:

  • Limited elbow rotation or forearm movement
  • Difficulty turning palms up or down
  • Family history of radioulnar synostosis or similar bone conditions
  • Unexplained forearm stiffness or joint limitations
  • Planning for family and concerned about genetic inheritance

Many South Africans live with these symptoms without understanding their genetic origins. Early detection through genetic testing can help manage the condition more effectively and prevent complications.

Why This Test Matters for Your Health Journey

Getting the right diagnosis is the first step toward effective management. This test offers:

  • Accurate Diagnosis: Eliminate uncertainty with precise genetic confirmation
  • Family Planning Insights: Understand inheritance patterns for future generations
  • Treatment Guidance: Help your orthopaedic specialist develop targeted treatment plans
  • Peace of Mind: Reduce anxiety by understanding your genetic profile
  • Early Intervention: Identify conditions before they cause significant limitations

Understanding Your Test Results

We understand that genetic test results can be overwhelming. That’s why every test includes comprehensive genetic counselling to help you understand your results clearly. Our genetic counsellors will:

  • Explain your results in simple, understandable language
  • Discuss what the findings mean for your health
  • Help you understand inheritance patterns and family implications
  • Provide guidance on next steps and specialist referrals
  • Answer all your questions with patience and expertise

You’ll receive a detailed report that you can share with your healthcare provider, ensuring coordinated care and appropriate treatment planning.

Affordable Genetic Testing for South Africans

Service Regular Price Special Price
FGFRL1 Gene Radioulnar Synostosis NGS Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session Included at no extra cost
Family Pedigree Analysis Included at no extra cost
Results Interpretation Included at no extra cost

Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card

Why Trust Oracle Genomics?

As South Africa’s leading genetic testing provider, we combine medical expertise with compassionate care:

  • Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Advanced Technology: State-of-the-art NGS technology for unparalleled accuracy
  • Expert Team: Board-certified geneticists and counsellors
  • Patient-First Approach: We prioritize your understanding and comfort
  • Proven Track Record: Thousands of satisfied patients nationwide

Take the First Step Toward Understanding Your Bone Health

Don’t let uncertainty about your forearm condition hold you back. Early genetic testing can provide the answers you need to manage your health effectively. Our special pricing of ZAR 6,700 makes this advanced testing accessible to more South Africans.

Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Take advantage of this opportunity to get comprehensive genetic insights at an affordable price.

“The clarity from my genetic test changed everything. Finally understanding my condition helped me and my doctor create an effective treatment plan.” – Recent Patient