Test Price
2,800 AED✅ Home Collection Available
C21orf2 Gene Cone-Rod Dystrophy Genetic Test in UAE | 2800 AED | DHA Licensed Facility
Executive Summary & Core Metrics
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited NGS processing (Cert: INT/EGQ/2509DA/3139), fully aligned with DHA clinical guidelines.
- ✓ Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM. Sample types: whole blood or DNA FTA card.
- ✓ Clinical Guidance: Complimentary telephonic post‑test genetic counseling to interpret results in the context of your family history and ophthalmological findings.
- ✓ Insurance & Billing: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The C21orf2 gene test identifies pathogenic variants causing cone‑rod dystrophy, a progressive inherited retinal disorder affecting central and peripheral vision. By sequencing the entire coding region of C21orf2 and over 30 associated retinal genes using next‑generation sequencing (NGS), this test provides a definitive molecular diagnosis, guiding prognosis and family planning.
| Feature | Our Test (NGS Panel) | Single‑Gene Sanger Sequencing |
|---|---|---|
| Gene Coverage | Full C21orf2 gene + 30+ retinal dystrophy genes | Only C21orf2 coding regions |
| Detection Depth | >200× mean depth, >99.9% sensitivity | ~100× coverage, possible false negatives |
| Turnaround Time | 3 – 4 weeks | 4 – 6 weeks |
| Price | 2,800 AED | Often 2,500 – 3,000 AED (limited scope) |
| Regulatory Compliance | ISO 9001:2015, DHA Licensed Facility 1143 | Variable |
Physician Insight & Safety Protocols
“A positive C21orf2 result confirms the genetic basis of your cone‑rod dystrophy, but it must be interpreted alongside a comprehensive retinal examination and detailed family pedigree. Genetic information is permanent; our role is to ensure you fully understand what it means for your vision, your children, and your future care. We guide you through each result with clarity and compassion.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
⚠️ Important Advisory
Do not discontinue any prescribed medication or vitamin supplement without consulting your treating ophthalmologist or physician. Your eye health management plan must remain unchanged until all test results are discussed during your post‑test genetic counseling session.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Bone marrow transplant recipients (allogeneic) due to potential chimerism that may invalidate genetic results. Patients with known large‑scale genomic rearrangements interfering with NGS should discuss alternative methods with our genetic counselor.
- Immediate ER Red Flags: If you experience sudden vision loss, severe eye pain, flashes of light, or a curtain‑like shadow in your field of vision, seek emergency ophthalmic care immediately. This test is not a substitute for acute clinical evaluation.
- All samples are processed under the UAE Personal Data Protection Law (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, ensuring full confidentiality and informed consent.
Patient FAQ & Clinical Guidance
1. What does the C21orf2 gene test detect, and why is it essential for cone‑rod dystrophy diagnosis?
It identifies pathogenic DNA mutations in the C21orf2 gene that cause cone‑rod dystrophy, providing a definitive molecular diagnosis that confirms the clinical suspicion and aids in predicting disease progression.
2. How is the sample collected, and can I use a painless FTA card at home?
Our VIP mobile phlebotomist collects a few drops of blood from a finger prick onto an FTA card, or a venous blood sample, all handled with temperature‑controlled cold‑chain integrity. The process is minimally invasive and can be scheduled between 8 AM and 11 PM via WhatsApp.
3. Will my insurance cover this genetic test, and how can I verify coverage?
Many UAE‑based insurers cover medically indicated genetic tests for inherited retinal diseases; our billing team performs direct verification within 2 hours when you send your Emirates ID and insurance card via WhatsApp to +971 54 548 8731.
4. How long will it take to get my results, and what do they include?
Results are typically available within 3 to 4 weeks from sample receipt. Your comprehensive report includes variant classification, clinical interpretation, and inheritance risk assessment, all discussed during your follow‑up genetic counseling appointment.
UAE Regulatory & Data Privacy Adherence
This diagnostic service operates under the DHA Facility License Number 1143, located at Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. We strictly adhere to 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. Clinical testing safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. All genetic data is handled with encryption and access controls ensuring full confidentiality.
Clinical & Logistical Metadata
| Test Name | C21orf2 Gene Cone-Rod Dystrophy Genetic Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3 – 4 weeks |
| Sample Type / Matrix | Whole blood or DNA FTA card (peripheral blood) |
| Methodology Used | Next‑Generation Sequencing (NGS) – targeted gene panel |
| ICD-10-CM Code | H35.53 (Cone‑rod dystrophy) |
| LOINC Code | 21636-6 (Genetic analysis, DNA) |
| DHA Facility License & Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
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
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians