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EYA1 Gene Branchiootorenal Syndrome Type 1 NGS Genetic DNA Test

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

-28%

Facing concerns about hereditary hearing loss, kidney issues, or branchial arch abnormalities in your family? The EYA1 Gene Branchiootorenal Syndrome Type 1 NGS Genetic DNA Test provides definitive answers and peace of mind. For only R6,700 (regularly R9,350), this advanced Next-Generation Sequencing test detects mutations in the EYA1 gene that cause this complex inherited disorder affecting multiple body systems. Our comprehensive testing includes professional genetic counselling to map your family history and understand your specific risks. With results in just 3-4 weeks, you can make informed decisions about your family’s health future. Oracle Genomics offers nationwide coverage across South Africa, including convenient testing locations in Johannesburg, Cape Town, Durban, and Pretoria. Take control of your genetic health journey with confidence and accuracy.

📞 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

EYA1 Gene Test R6
EYA1 Gene Branchiootorenal Syndrome Type 1 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Family’s Genetic Health Journey

When hereditary conditions like hearing loss, kidney abnormalities, or branchial arch defects run in your family, the uncertainty can be overwhelming. The EYA1 Gene Branchiootorenal Syndrome Type 1 NGS Genetic DNA Test offers clarity and confidence for South African families navigating complex genetic health concerns. Our compassionate approach combines cutting-edge technology with professional genetic counselling to provide the answers you need for informed family planning and proactive healthcare decisions.

What This Advanced Genetic Test Detects

The EYA1 gene plays a crucial role in embryonic development, particularly affecting the ears, kidneys, and branchial arches. Mutations in this gene can lead to Branchiootorenal Syndrome Type 1, a complex condition that may involve hearing loss, kidney malformations, and distinctive facial features. Our Next-Generation Sequencing (NGS) technology provides comprehensive analysis of the EYA1 gene, identifying even subtle genetic variations that could impact your family’s health across generations.

Who Should Consider This Genetic Screening?

This test is particularly important if you or your family members experience:

  • Unexplained hearing loss, especially if present from childhood
  • Family history of kidney abnormalities or renal issues
  • Branchial arch defects or unusual neck cysts/sinuses
  • Multiple family members with similar ear, kidney, or facial features
  • Planning pregnancy with concerns about hereditary conditions
  • Unexplained developmental delays in children

Early detection through genetic testing can transform your family’s healthcare journey, providing clarity and enabling proactive management strategies.

Why Genetic Clarity Matters for Your Family’s Future

Understanding your genetic profile offers profound benefits for your entire family:

  • Peace of Mind: Eliminate uncertainty about hereditary risks
  • Informed Family Planning: Make confident decisions about future pregnancies
  • Early Intervention: Enable timely medical management for affected family members
  • Comprehensive Care: Coordinate appropriate specialist care based on genetic findings
  • Generational Impact: Protect future generations through genetic awareness

Understanding Your Genetic Results with Compassion

Receiving genetic test results can feel overwhelming, which is why our approach focuses on clarity and support. Your results will be presented in a comprehensive report that explains:

  • Specific genetic variations detected in the EYA1 gene
  • What these findings mean for your health and family
  • Recommended next steps and specialist consultations
  • Family planning considerations and recurrence risks
  • Available support resources and management options

Our genetic counsellors are available to help you understand your results and navigate the implications for your family’s health journey.

Transparent Pricing for Genetic Peace of Mind

Service Regular Price Special Price Savings
EYA1 Gene Branchiootorenal Syndrome Type 1 NGS Test R9,350 R6,700 R2,650
Includes Genetic Counselling Session Comprehensive family history assessment and pedigree chart
Turnaround Time 3-4 weeks for complete results

Consider this investment in your family’s genetic health as proactive protection against future healthcare costs and emotional uncertainty.

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Convenient testing locations across Johannesburg, Cape Town, Durban, Pretoria and major centres
  • Medical Expertise: Collaboration with leading ophthalmologists and genetic specialists
  • Advanced Technology: Next-Generation Sequencing for unparalleled accuracy
  • Professional Support: Comprehensive genetic counselling included with every test
  • Proven Reliability: Trusted by healthcare professionals across South Africa

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about hereditary conditions cloud your family’s future. With our special pricing of R6,700 and comprehensive genetic counselling, you can gain the clarity needed to make informed healthcare decisions.

Book Your Genetic Counselling Session Now:

  • Call our dedicated genetic health line: [Phone Number]
  • Visit our website to schedule online: [Website URL]
  • Email our genetic counselling team: [Email Address]

Early detection through genetic testing can transform your family’s healthcare journey. Take control of your genetic health with confidence and professional support from Oracle Genomics.