Test Price
2,800 AED✅ Home Collection Available
CFAP298 Gene Primary Ciliary Dyskinesia Type 26 Genetic Test in UAE | 2,800 AED | 2026 DHA Guidelines
تحليل جين CFAP298 للخلل الهدبي الأولي من النوع 26 بتقنية التسلسل الجيني المتقدم (NGS) في الإمارات | 2,800 درهم | معتمد من هيئة الصحة بدبي
ملخص تنفيذي: يقدم فحص جين CFAP298 بتقنية التسلسل الجيني الشامل (NGS) تشخيصًا جينيًا دقيقًا للخلل الهدبي الأولي من النوع 26، مع ضمان دقة 99.9% عبر مختبر معتمد وفق ISO، وجمع عينات منزلية تحت إشراف طبي، وإرشاد سريري هاتفي بعد ظهور النتيجة.
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- ✓ Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain.
- ✓ Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Comprehensive Genetic Diagnosis for Primary Ciliary Dyskinesia Type 26
The CFAP298 Genetic Test identifies pathogenic variants in the CFAP298 gene responsible for primary ciliary dyskinesia type 26 (PCD26), a rare autosomal recessive disorder characterised by chronic otitis media, rhinosinusitis, and progressive bronchiectasis. يُعد هذا التحليل الجيني الأكثر دقة لتأكيد التشخيص السريري وتوجيه خطة رعاية شاملة.
| Feature | Our CFAP298 NGS Test | Closest Alternative (Panel/Limited Sequencing) |
|---|---|---|
| Precision | Full gene sequencing (99.9% analytical sensitivity) | Selected exons only; may miss novel or deep intronic variants |
| Method | NGS (Illumina NovaSeq) + Sanger confirmation | Sanger sequencing or targeted panel with limited coverage |
| Turnaround | 3 to 4 weeks | Often 5–6 weeks or unevaluable for full gene |
Sample Requirements & Pre-Test Preparation
Accepted Sample Types:
- Whole blood (EDTA tube, 2–5 mL)
- Extracted DNA (≥1 µg, concentration ≥20 ng/µL)
- One drop of blood on FTA card (properly dried)
Pre-Test Recommendations:
A detailed clinical history including chronic/recurrent upper and lower respiratory infections, neonatal respiratory distress, otitis media, sinusitis, or situs inversus should be provided. Genetic counselling is strongly advised to draw a comprehensive pedigree chart of potentially affected family members before testing. No specific medication or supplement avoidance is required; however, if the patient has received a whole blood transfusion or allogeneic bone marrow transplant within the last 90 days, please inform our team as donor DNA may interfere.
Physician Insight & Safety Protocol
“As a clinician, I understand the anxiety associated with unexplained recurrent infections. This test provides a definitive molecular diagnosis, allowing proper surveillance and multidisciplinary care. Please remember that a negative result does not exclude all ciliary disorders, and clinical correlation remains essential. We are here to guide you through the entire process.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011, Clinical Genomics & ENT Specialist
⚠️ Do not discontinue prescribed medication without consulting your doctor.
🛑 Exclusion Criteria & Emergency Red Flags
- Not suitable for: individuals who have received a recent whole blood transfusion or allogeneic bone marrow transplant (≤90 days) as donor DNA may confound results.
- Seek emergency care immediately (call 998) if the patient develops acute respiratory distress, high fever with cyanosis, or syncope; this genetic test is not intended for acute diagnosis.
- Testing is not recommended for asymptomatic minors without parental consent and formal genetic counselling, in accordance with UAE CDS Law 2026.
Unmatched Accuracy & UAE Regulatory Compliance
99.9% Diagnostic Sensitivity
Our NGS assay targets all coding exons and ±20 bp flanking intronic regions, complemented by Sanger confirmation for detected variants, achieving unparalleled analytical sensitivity. Method validated per ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).
Home Collection & Cold-Chain Logistics
VIP mobile phlebotomy available 8 AM – 11 PM daily. Samples are transported at 2–8°C using ISO-certified cold-chain protocols to guarantee DNA integrity. WhatsApp +971 54 548 8731 to schedule.
Full UAE Legal & Data Privacy Compliance
This service strictly adheres to Federal Decree-Law No. 41 of 2024 on Medical Liability (Art. 87), CDS Law 2026 (genetic testing on minors requires guardian consent and counselling), and the UAE Personal Data Protection Law (PDPL). All patient data is encrypted, stored on secure servers, and never shared without explicit consent.
Patient FAQ & Clinical Guidance
1. What is the CFAP298 gene test, and why is it recommended?
Snippet-grade answer: The CFAP298 NGS test diagnoses primary ciliary dyskinesia type 26, a rare genetic disorder causing chronic ear, sinus, and lung infections. It identifies disease-causing mutations in the CFAP298 gene, enabling early targeted intervention. A positive result guides tailored respiratory care and fertility counselling.
سؤال وجواب سريري: تحليل جين CFAP298 يشخص الخلل الهدبي الأولي من النوع 26، وهو مرض وراثي نادر يسبب التهابات مزمنة في الأذن والجيوب الأنفية والرئتين. يكشف التحليل عن الطفرات المسببة للمرض في جين CFAP298، مما يساعد في بدء الرعاية التنفسية الموجهة والاستشارة الوراثية.
2. How is the sample collected, and how long will results take?
Snippet: A simple blood draw or a drop on an FTA card is collected at home by our certified phlebotomist; results are ready in 3–4 weeks. The process is virtually painless and requires no fasting. You receive a comprehensive molecular report interpreted by our clinical geneticists.
تُجمَع العينة بسهولة في المنزل عبر سحب دم بسيط أو قطرة دم على بطاقة FTA، وتصدر النتائج خلال 3–4 أسابيع. العملية غير مؤلمة ولا تستدعي الصيام، مع تقرير جيني شامل مفسر من قبل استشاريين.
3. Do I need a doctor’s referral or genetic counselling before this test?
Snippet: Yes, a doctor’s referral and pre- genetic counselling are mandatory to ensure clinical appropriateness and informed consent. Our team arranges a teleconsultation with a DHA-licensed genetic counsellor prior to sample collection. This meeting explains the inheritance pattern, possible outcomes, and implications for family members.
نعم، الإحالة الطبية والاستشارة الوراثية السابقة للفحص إلزامية لضمان الملاءمة السريرية والموافقة المستنيرة. فريقنا يرتب استشارة هاتفية مع مستشار وراثي مرخص من هيئة الصحة بدبي قبل جمع العينة لشرح نمط الوراثة والنتائج المحتملة.
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