Test Price
2,800 AED✅ Home Collection Available
DYX1C1 Gene Primary Ciliary Dyskinesia Type 25 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين DYX1C1 لخلل الحركة الهدبية الأولي من النوع 25 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
دقة تشخيصية 99.9% عبر سلسلة التبريد المعتمدة ISO
خدمة سحب الدم المنزلية الفاخرة والمعتمدة من هيئة الصحة
التوجيه السريري بعد الفحص عبر الهاتف
التحقق المباشر من التأمين عبر واتساب +971 54 548 8731
Accuracy: 99.9% Diagnostic Sensitivity via ISO-Accredited Cold-Chain Processing.
Premium Logistics: Hospital-Grade Home Collection with VIP Mobile Phlebotomy.
Clinical Guidance: Telephonic Post-Test Result Interpretation by Clinical Experts.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Clinical Utility
The DYX1C1 gene test detects pathogenic variants causing Primary Ciliary Dyskinesia Type 25 (PCD25), a rare genetic disorder marked by chronic respiratory infections, infertility, and laterality defects. تحليل الجين DYX1C1 يكشف الطفرات المسببة لخلل الحركة الهدبية الأولي من النوع 25، وهو اضطراب وراثي نادر يتسم بالتهابات الجهاز التنفسي المزمنة والعقم.
This comprehensive NGS assay provides definitive molecular diagnosis, guiding personalized treatment and family planning.
| Feature | Our Test (DYX1C1 NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | >99% analytical sensitivity & specificity; full gene coverage | Limited to known hotspots, lower variant detection |
| Method | Next-Generation Sequencing (NGS) with bioinformatic validation | Capillary electrophoresis; may miss copy number variations |
| Turnaround | 3–4 weeks | 4–6 weeks |
Physician Insight & Safety Protocol
“As a clinical geneticist (DHA: 61713011), I emphasize that a positive DYX1C1 result must be correlated with full clinical phenotype and family history; early molecular diagnosis allows proactive management of respiratory complications and fertility counseling.”
“This test is a powerful guide, but it never replaces comprehensive clinical evaluation. Please share your report with your treating ENT and pulmonologist.”
⚠️ Important Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Genetic results do not alter acute treatment plans without clinical review.
Exclusion Criteria & Urgent Red Flags
- Active severe systemic infection or fever >38.5°C – test should be deferred.
- Recent blood transfusion (within 2 weeks) – may interfere with DNA purity.
- Pregnant minors (<18 years) without court-appointed guardian consent per UAE CDS Law 2026.
- Seek ER if after sample collection you experience: sudden breathlessness, chest pain, cyanosis, or heavy uncontrolled bleeding.
Patient FAQ & Clinical Guidance
Q1: What does the DYX1C1 genetic test detect?
Snippet: The DYX1C1 NGS finds mutations linked to primary ciliary dyskinesia type 25 for precise clinical diagnosis.
It sequences the entire coding region of the DYX1C1 gene, identifying missense, nonsense, splicing variants, and small deletions. A positive result confirms the molecular basis of PCD25, enabling targeted screening of family members and early intervention with airway clearance therapies.
يكشف اختبار DYX1C1 عبر الجيل التالي الطفرات المسببة لخلل الحركة الهدبية الأولي من النوع 25 لتأكيد التشخيص السريري بدقة.
Q2: What sample types are accepted?
Snippet: Options: blood, extracted DNA, or single blood drop on FTA card; VIP home collection available.
We accept whole blood collected in EDTA tubes, previously extracted DNA (concentration >20 ng/µL), or a simple dried blood spot on an FTA card. A DHA-licensed phlebotomist arrives equipped with validated cold-chain material for home collection between 8 AM and 11 PM, ensuring sample stability.
خيارات العينة: دم وريدي، حمض نووي مستخلص، أو نقطة دم واحدة على بطاقة FTA مع خدمة سحب منزلي متميزة.
Q3: How soon will I receive my results?
Snippet: Results ready in 3 to 4 weeks, with telephonic clinical guidance for your doctor's interpretation.
The complex NGS workflow—library preparation, sequencing, variant calling, and Sanger confirmation—requires 3–4 weeks. A board-certified geneticist reviews every report. On delivery, we offer a complimentary telephonic session to discuss findings and next steps with your referring physician.
تظهر النتائج في غضون 3 إلى 4 أسابيع، مع توجيه سريري هاتفي بعد الاستلام لتفسير طبيبك.
Compliant with UAE Federal Decree-Law No. 41 of 2024 (Article 87), CDS Law 2026 (Minors), and UAE PDPL. ISO 9001:2015 Certified (INT/EGQ/2509DA/3139).
DHA Facility License: 9834453 | Clinical Review: Dr. Prabhakar Reddy, DHA 61713011 | LOINC: 93385-3 | ICD-10-CM: Q34.8, Z15.01, Z82.79
For direct billing verification or to schedule VIP home collection: +971 54 548 8731 (WhatsApp).
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Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
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All reports reviewed by DHA-Certified physicians