Test Price
2,800 AED✅ Home Collection Available
CCDC114 Gene Primary Ciliary Dyskinesia Genetic Test (NGS) in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
Executive Summary
Our center offers an advanced genetic test for the CCDC114 gene using next-generation sequencing (NGS), with diagnostic accuracy of 99.9% and DHA-licensed standards. The test includes a premium home collection service by licensed nurses with ISO-certified cold-chain shipping, and post-test telephonic clinical guidance by a DHA-licensed consultant. The price is 2800 AED with direct insurance billing. Contact WhatsApp +971 54 548 8731 for verification.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing (ISO 9001:2015 Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy service (8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by a DHA-licensed consultant.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The CCDC114 gene test employs next-generation sequencing to detect pathogenic variants responsible for Primary Ciliary Dyskinesia type 20, a rare genetic disorder causing chronic sino-pulmonary infections, laterality defects, and infertility. This advanced genetic test confirms the diagnosis and assists in genetic counseling and family planning.
Pre-test Information: Prior to testing, a detailed clinical evaluation is recommended, including documentation of recurrent otitis media, sinusitis, bronchiectasis, and situs abnormalities. A genetic counselling session to draw a pedigree chart of family members affected by primary ciliary dyskinesia is strongly advised.
| Feature | Our CCDC114 NGS Test | Closest Alternative |
|---|---|---|
| Methodology | Next‑Generation Sequencing (NGS) – full gene analysis | Targeted mutation panel (limited coverage) |
| Diagnostic Precision | 99.9% sensitivity, ISO‑validated, DHA aligned | Variable; may miss rare CCDC114 variants |
| Turnaround Time | 3–4 weeks | 4–6 weeks |
| Price | 2800 AED | Inquire (often higher) |
| Home Collection | ✔ ISO‑cooled chain, 8 AM–11 PM | May not be available |
| Post‑Test Clinical Support | ✔ Free tele‑guidance from DHA specialist | Limited or none |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA License: 9294403 – “Genetic confirmation of CCDC114‑related primary ciliary dyskinesia must be interpreted alongside thorough clinical phenotyping—recurrent ear, sinus, and lung infections often beginning in infancy, plus laterality defects. This test provides clarity for affected families and guides early interventions, but it does not replace a detailed physical evaluation and specialist follow‑up. Always involve a multidisciplinary team (ENT, pulmonologist, clinical geneticist) in the diagnostic journey.”
Medication Advisory
Do not discontinue prescribed medication (e.g., antibiotics, mucolytics, bronchodilators) without consulting your treating physician. Genetic testing does not constitute a treatment pause; ongoing management of respiratory symptoms remains essential.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Blood transfusion within 21 days prior to sampling, use of heparin as the sole anticoagulant (EDTA or citrate acceptable), or a dried FTA card that has not been properly desiccated. Unconscious or unstable patients are not eligible for home collection; seek hospital-based care.
- Emergency Red Flags: Sudden worsening of respiratory distress, cyanosis, high fever with chest pain, or acute pneumonia – proceed to the nearest Emergency Department immediately. This genetic test is an elective diagnostic tool and not for acute management.
Patient FAQ & Clinical Guidance
1. What is the CCDC114 gene test, and why is it needed?
This test analyzes the CCDC114 gene via NGS to detect mutations causing primary ciliary dyskinesia type 20, which leads to chronic respiratory infections. It is recommended for individuals with a clinical suspicion of PCD, including situs inversus, neonatal respiratory distress, or persistent wet cough, and for family members to assess carrier status and guide reproductive decisions.
2. How is sample collection performed, and is home collection available?
A simple blood draw, DNA extraction from cheek swab, or a blood spot on an FTA card is required, with home collection available across the UAE. Our cold-chain certified phlebotomists visit between 8 AM and 11 PM, ensuring sample integrity from your doorstep to our ISO-accredited laboratory.
3. How long do results take, and what is the cost?
Results are typically ready within 3 to 4 weeks, and the test costs 2800 AED with direct insurance verification. The price includes pre‑test counselling, laboratory analysis, a comprehensive report, and one post‑telephonic clinical interpretation session.
UAE Regulatory & Data Privacy Adherence
Data Protection: All patient data is handled in compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Your genetic information is encrypted and accessed only by authorized personnel.
Clinical Safety: This test follows the guidelines of Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring patient consent is obtained and clinical safety is prioritized.
Clinical & Logistical Metadata
| Test Name | CCDC114 Gene Primary Ciliary Dyskinesia Genetic Test (NGS) |
| Price (AED) | 2800 |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Whole Blood, Buccal Swab, or Dried Blood Spot |
| Methodology Used | Next-Generation Sequencing (NGS) – Full Gene Analysis |
| ICD-10-CM Code | Q34.8 |
| LOINC Code | 94807-4 |
| DHA Facility License & Laboratory Address | License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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