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OCRL Gene Lowe Oculocerebrorenal Syndrome NGS Genetic DNA Test

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

-28%

Facing concerns about Lowe oculocerebrorenal syndrome? Our comprehensive OCRL gene DNA test provides the clarity you need for just ZAR 6,700. This advanced NGS genetic test detects mutations in the OCRL gene that cause this rare but serious condition affecting eyes, brain, and kidneys. Early detection through our precise testing can help you understand your genetic risk, make informed family planning decisions, and access appropriate medical care sooner. We understand the anxiety that comes with genetic concerns, which is why our test includes professional genetic counselling to help you understand your results and their implications. Available nationwide across South Africa, our trusted testing process delivers results within 3-4 weeks, giving you the peace of mind and actionable information you deserve for your family’s health journey.

📞 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

OCRL Gene Lowe Syndrome DNA Test | ZAR 6
OCRL Gene Lowe Oculocerebrorenal Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Lowe Oculocerebrorenal Syndrome

When you’re concerned about a rare genetic condition that affects multiple body systems, the uncertainty can feel overwhelming. Our OCRL gene DNA test provides the answers you need to understand your genetic risk and take control of your family’s health journey. For South African families in Johannesburg, Cape Town, Durban, and Pretoria, we offer trusted genetic testing that brings peace of mind and clear direction.

Understanding the OCRL Gene Test

This advanced Next-Generation Sequencing (NGS) test specifically examines the OCRL gene for mutations that cause Lowe oculocerebrorenal syndrome. This rare condition affects the eyes (cataracts), brain (developmental delays), and kidneys (renal dysfunction). Our test provides comprehensive analysis using the latest genetic technology, ensuring you receive the most accurate results possible.

We make complex genetic information accessible and understandable. The test requires either a blood sample, extracted DNA, or a simple blood drop on an FTA card, making the process convenient and minimally invasive.

Who Should Consider This Test?

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

  • Infants born with cataracts or eye abnormalities
  • Developmental delays in early childhood
  • Kidney problems or renal dysfunction
  • Family history of Lowe syndrome
  • Planning pregnancy with known family risk factors
  • Unexplained neurological symptoms in children

Early detection can significantly impact treatment outcomes and quality of life management.

Why This Test Matters for Your Family’s Health

Getting tested provides crucial benefits that extend beyond simple diagnosis:

  • Early Intervention: Identify the condition early to start appropriate treatments and therapies
  • Family Planning: Make informed decisions about future pregnancies
  • Peace of Mind: Reduce uncertainty and anxiety about genetic risks
  • Medical Management: Work with healthcare providers to create targeted care plans
  • Genetic Counselling: Understand inheritance patterns and family implications

Understanding Your Results

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

  • Clear Explanations: Results presented in easy-to-understand language
  • Professional Support: Genetic counselling included to discuss implications
  • Family Pedigree: Visual mapping of family genetic patterns
  • Next Steps Guidance: Clear recommendations based on your results
  • Medical Referrals: Connections to appropriate specialists if needed

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

Transparent Pricing – Exceptional Value

Service Regular Price Special Price
OCRL Gene Lowe Syndrome NGS Test ZAR 9,350 ZAR 6,700
Includes genetic counselling and comprehensive result interpretation

Considering the potential healthcare costs of undiagnosed genetic conditions, this test represents significant long-term value for your family’s health.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Advanced Technology: Latest NGS technology for maximum accuracy
  • Expert Team: Qualified genetic specialists and counsellors
  • Quick Turnaround: Results within 3-4 weeks
  • Patient-Focused: Empathetic support throughout your journey
  • Clinical Excellence: Partnered with general physicians for comprehensive care

Take the First Step Toward Genetic Clarity

Don’t let uncertainty about Lowe syndrome affect your family’s future. Our comprehensive testing provides the answers you need to make informed health decisions.

Limited Time Offer: Save ZAR 2,650 on this essential genetic screening. Early detection can make all the difference in managing health outcomes.