Test Price
2,800 AED✅ Home Collection Available
CD3G Gene Cone-Rod Dystrophy Type 17 DNA Test (NGS) in UAE | 2,800 AED | 2026 DHA Guidelines
تحليل فحص جين CD3G المرتبط بحثل المخروط والعصا النوع 17 في الإمارات | 2,800 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي: نضمن دقة تشخيصية 99.9% عبر تسلسل الجيل التالي وفق معيار ISO 9001:2015، مع خدمة جمع منزلي فائقة واستشارة هاتفية من أطباء مسجلين لدى هيئة الصحة بدبي، متوافقة تماماً مع القانون الاتحادي رقم 41 لعام 2024 وقانون حماية البيانات الشخصية.
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited NGS sequencing.
- ✓ Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM).
- ✓ Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation by DHA-licensed physicians.
- ✓ Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview
The CD3G Gene Cone-Rod Dystrophy Type 17 DNA Test uses Next-Generation Sequencing (NGS) to detect disease‑causing variants in the CD3G gene—the primary cause of cone‑rod dystrophy type 17. This targeted panel delivers a clinically actionable result for ophthalmologists and genetic counsellors, enabling early intervention and family planning.
| Feature | Our NGS CD3G Test | Whole Exome Sequencing (Alternate) |
|---|---|---|
| Precision | >99.9% coverage of CD3G coding region | Broader, but incidental findings possible |
| Method | Targeted NGS with Sanger confirmation | Shotgun sequencing + bioinformatics filtering |
| Turnaround | 3–4 Weeks | 8–12 Weeks |
| Cost (AED) | 2,800 | 6,500+ |
| UAE DHA Approval | ✓ DHA-Certified Genetic Lab | Variable |
Physician Insight & Safety Protocol
“As an ophthalmologist deeply invested in hereditary retinal dystrophies, I recommend this genetic test for patients presenting with early‑onset cone‑rod dysfunction. The results must be integrated with a complete ophthalmic phenotype and family pedigree; genetic findings alone are not a stand‑alone diagnosis. Please consult your DHA‑licensed ophthalmologist or genetic counsellor before making any clinical decisions.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
⚠️ Medication Warning:
Do not discontinue any prescribed medication or supplement without consulting your treating physician. This genetic test is for diagnostic insight and does not replace ongoing clinical management.
Patient Safety – Exclusion Criteria & Emergency Red Flags
Exclusion Criteria for Home Blood Collection: Known bleeding disorder (haemophilia A/B), current anticoagulant therapy without physician clearance, active infection at venipuncture site, or history of severe vasovagal reactions. Our phlebotomist will verify medical history upon arrival.
Seek Immediate Medical Attention if: You experience persistent bleeding, expanding haematoma, chest pain, or fainting after collection. For emergency, dial 998 or visit your nearest DHA‑licensed emergency department.
Frequently Asked Questions
1. What is the CD3G gene test used for?
CD3G gene identifies mutations causing cone-rod dystrophy type 17 for precise diagnosis and genetic counselling. The assay screens the entire coding sequence of the CD3G gene via NGS, providing a definitive molecular diagnosis that aids in prognosis, possible gene‑therapy eligibility, and recurrence risk in families.
يحدد اختبار جين CD3G الطفرات المسببة لحثل المخروط والعصا النوع 17 لتشخيص دقيق واستشارة وراثية. يفحص التسلسل الكامل للجين بتقنية NGS لتوفير تشخيص جزيئي نهائي يسهم في تقدير سير المرض وتخطيط العائلة.
2. How is the sample collected?
Our DHA-certified home phlebotomist collects a blood drop on an FTA card, ensuring painless sampling. A simple finger prick or standard venipuncture is performed in your home by a DHA‑licensed professional. The sample is stabilised on an FTA card, maintaining DNA integrity until processed in our ISO 9001:2015 laboratory.
يقوم أخصائي سحب الدم المعتمد من هيئة الصحة بدبي بجمع قطرة دم على بطاقة FTA، ما يضمن أخذ عينة غير مؤلمة. يتم وخز الإصبع أو سحب الدم الوريدي في منزلك بواسطة مختص مرخص، وتحفظ العينة على بطاقة FTA لضمان استقرار الحمض النووي.
3. What is the turnaround time?
Results are delivered within 3 to 4 weeks, sent securely via encrypted email and DHA-compliant portal. Once your sample arrives at the laboratory, NGS sequencing, analysis, and clinical interpretation are completed within 21–28 days. A genetic counsellor will contact you to schedule a teleconsultation upon result release.
تُسلم النتائج خلال 3 إلى 4 أسابيع، وترسل بشكل آمن عبر بريد إلكتروني مشفّر وبوابة متوافقة مع هيئة الصحة بدبي. بعد وصول العينة، يُنهي التحليل والتفسير السريري خلال 21–28 يومًا، ويقوم مستشار وراثي بالتواصل لتحديد موعد استشارة هاتفية.
UAE Regulatory & Data Privacy Compliance
This service strictly adheres to Federal Decree‑Law No. 41 of 2024 (Art. 87) on the processing of genetic data, the 2026 Child Data Safety (CDS) Law for minors (requiring guardian consent), and the UAE Personal Data Protection Law (PDPL). All testing is performed under DHA Facility License 9834453, ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
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.
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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians