Sale!

FGFR1 Gene Craniosynostosis NGS Genetic DNA Test

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

-28%

If you’re concerned about your child’s skull development or family history of craniosynostosis, our FGFR1 Gene Craniosynostosis NGS Genetic DNA Test provides the answers you need. For only ZAR 6,700 (regularly ZAR 9,350), this advanced test uses Next Generation Sequencing technology to detect FGFR1 gene mutations that cause abnormal skull fusion in infants and children. Our test offers early detection that can guide treatment decisions and prevent complications. With results in just 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, and Durban, you can trust Oracle Genomics for accurate, reliable genetic testing that puts your family’s health first. We understand the anxiety that comes with genetic concerns, which is why we include genetic counselling to help you understand your results and make informed decisions.

📞 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

FGFR1 Craniosynostosis DNA Test | ZAR 6
FGFR1 Gene Craniosynostosis 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”]

Understanding Your Child’s Skull Development: FGFR1 Craniosynostosis DNA Testing

As a parent, noticing anything unusual about your baby’s head shape or development can be deeply concerning. That persistent worry about whether your child’s skull is forming properly, the questions about family history, and the fear of what might be causing those abnormal head shapes – we understand these anxieties completely. At Oracle Genomics, we’re here to provide the clarity and answers you need through our specialised FGFR1 Gene Craniosynostosis NGS Genetic DNA Test.

What This Test Detects: Your Path to Clarity

The FGFR1 gene plays a crucial role in normal skull development during infancy. When mutations occur in this gene, it can lead to craniosynostosis – a condition where the skull bones fuse together too early, preventing proper brain growth and causing abnormal head shapes. Our advanced Next Generation Sequencing (NGS) technology examines the FGFR1 gene with exceptional accuracy, identifying even the smallest genetic variations that could be affecting your child’s development.

Is This Test Right for Your Family?

This test is particularly important if your child shows:

  • Unusual head shape or asymmetry
  • Ridges along the skull sutures
  • Slow head growth despite normal body growth
  • Family history of craniosynostosis or genetic disorders
  • Developmental delays that might relate to skull pressure

Many South African families in Johannesburg, Cape Town, and Durban have found peace of mind through early genetic testing, allowing for timely interventions when needed.

Why Early Detection Matters for Your Child’s Future

Early identification of FGFR1 gene mutations provides numerous benefits:

  • Guided Treatment Planning: Results help paediatric specialists create targeted treatment strategies
  • Prevention of Complications: Early intervention can prevent increased intracranial pressure and developmental issues
  • Family Planning Insights: Understand inheritance patterns for future family planning decisions
  • Peace of Mind: Replace uncertainty with clear understanding and actionable information

Understanding Your Results: We’re Here to Guide You

Receiving genetic test results can feel overwhelming, which is why we include comprehensive genetic counselling with every test. Our specialists will:

  • Explain your results in clear, understandable language
  • Discuss what the findings mean for your child’s health
  • Create a pedigree chart to understand family inheritance patterns
  • Connect you with appropriate paediatric specialists if needed
  • Provide ongoing support for any questions that arise

Remember: A positive result doesn’t define your child’s future – it empowers you with knowledge to make the best healthcare decisions.

Transparent Pricing – Investing in Your Child’s Health

Service Regular Price Special Price Savings
FGFR1 Craniosynostosis NGS DNA Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Includes Genetic Counselling Complimentary with every test
Turnaround Time 3-4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Consider this: The cost of untreated craniosynostosis complications can far exceed the investment in early detection. Many medical schemes recognise the value of preventive genetic testing.

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing centres across South Africa, including major cities
  • Medical Expertise: Specialised in paediatric genetic conditions with years of experience
  • Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
  • Patient-Centred Care: We understand the emotional journey of genetic testing
  • Proven Track Record: Trusted by healthcare professionals throughout South Africa

Take the First Step Toward Answers Today

Don’t let uncertainty about your child’s development continue to cause worry. Every day matters when it comes to early detection and intervention.

Book Your Test Now

Secure your special pricing of ZAR 6,700 while available

Speak With Our Genetic Counsellor

Free consultation to discuss your concerns and whether this test is right for your family

Download Our Patient Guide

Comprehensive information about craniosynostosis and genetic testing

Limited Time Offer: Our special pricing of ZAR 6,700 represents significant savings off the regular ZAR 9,350 fee. This offer may not last, so we encourage you to take action while you can access this reduced rate.

“The clarity we gained from this test changed everything for our family. We finally had answers and could move forward with confidence.” – Parent from Pretoria