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CFAP298 Gene Primary Ciliary Dyskinesia Type 26 NGS Genetic DNA Test

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

-28%

If you or your child experience chronic respiratory infections, persistent cough, or breathing difficulties, our CFAP298 Gene Primary Ciliary Dyskinesia Type 26 test provides the answers you need. This comprehensive NGS genetic DNA test accurately detects mutations in the CFAP298 gene, helping diagnose this rare inherited condition that affects cilia function in the respiratory tract. For only ZAR 6,700 (special price from ZAR 9,350), you gain access to precise genetic analysis that can guide treatment decisions and improve quality of life. Our test delivers results within 3-4 weeks using advanced next-generation sequencing technology, ensuring the highest accuracy and reliability. Trust Oracle Genomics for professional genetic testing services available nationwide across South Africa, including Johannesburg, Cape Town, and Durban. Early detection through genetic testing can significantly impact respiratory health management and prevent complications.

📞 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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CFAP298 Gene PCD Test | ZAR 6
CFAP298 Gene Primary Ciliary Dyskinesia Type 26 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Answers for Chronic Respiratory Concerns with CFAP298 Gene Testing

Living with persistent respiratory symptoms can be exhausting and worrying. If you or your loved one experiences chronic cough, recurring infections, or breathing difficulties that don’t seem to improve, our CFAP298 Gene Primary Ciliary Dyskinesia Type 26 test offers the clarity you deserve. This advanced genetic test provides definitive answers about this rare inherited condition, helping you and your healthcare team make informed decisions about your respiratory health.

Understanding Your CFAP298 Gene Test

Primary Ciliary Dyskinesia (PCD) Type 26 is a genetic condition where the tiny hair-like structures called cilia in your respiratory tract don’t function properly. These cilia normally help clear mucus and debris from your airways, protecting you from infections. When the CFAP298 gene has mutations, it disrupts this vital cleaning system, leading to the chronic symptoms associated with PCD.

Our test uses Next-Generation Sequencing (NGS) technology to examine your CFAP298 gene with exceptional precision, identifying even subtle genetic changes that could be affecting your respiratory health.

Who Should Consider This Genetic Test?

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

  • Chronic cough that persists despite treatment
  • Recurrent respiratory infections (pneumonia, bronchitis)
  • Persistent nasal congestion and sinus infections
  • Breathing difficulties from early childhood
  • Family history of similar respiratory conditions
  • Unexplained fertility issues in adults (related to cilia function)

Many South African families have found answers through genetic testing when traditional diagnostic approaches couldn’t explain their persistent respiratory symptoms.

Why Early Detection Matters for Your Health

Getting a definitive diagnosis through CFAP298 gene testing can transform your approach to respiratory health management:

  • Personalised Treatment Plans: Your doctor can create targeted therapies specifically for PCD management
  • Prevent Complications: Early intervention can reduce lung damage and improve long-term outcomes
  • Family Planning Insights: Understand inheritance patterns for future family planning decisions
  • Peace of Mind: End the uncertainty and frustration of unexplained symptoms
  • Improved Quality of Life: Better management strategies can significantly enhance daily living

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. Our team provides clear, compassionate explanations of your results:

  • Positive Result: Indicates CFAP298 gene mutations were found. Our genetic counsellors will explain what this means for your health and next steps
  • Negative Result: No CFAP298 mutations detected, suggesting other causes for your symptoms
  • Uncertain Variants: Sometimes we find genetic changes with unclear significance – we’ll guide you through these findings

Your results come with comprehensive guidance and recommendations for discussing them with your ENT specialist or healthcare provider.

Affordable Genetic Testing for South African Families

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Limited time savings of ZAR 2,650
Turnaround Time 3-4 Weeks Prompt results for timely decisions
Sample Type Blood, Extracted DNA, or Blood on FTA Card Convenient collection options
Technology NGS (Next-Generation Sequencing) Gold standard accuracy

Consider this investment in your health: early diagnosis can prevent costly hospitalisations and reduce long-term healthcare expenses.

Why Trust Oracle Genomics for Your Genetic Testing?

We’ve built our reputation on accuracy, compassion, and accessibility for South African patients:

  • Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Specialised testing interpreted by experienced genetic professionals
  • Advanced Technology: State-of-the-art NGS technology ensures reliable results
  • Patient-Focused Care: We understand the emotional journey of genetic testing
  • Proven Accuracy: Rigorous quality control measures for every test

Take Control of Your Respiratory Health Today

Don’t let uncertainty about your respiratory symptoms continue affecting your quality of life. Our CFAP298 gene test provides the answers you need to move forward with confidence.

Book Your Test Now: Secure your special pricing of ZAR 6,700 while available

Multiple Collection Options: Choose blood draw or convenient FTA card sampling

Nationwide Accessibility: Available throughout South Africa with local support

Early detection through genetic testing can make a significant difference in managing Primary Ciliary Dyskinesia. Take the first step toward clearer answers and better respiratory health management.