Test Price
2,800 AED✅ Home Collection Available
CRB2 Gene (Ventriculomegaly–Cystic Kidney Disease) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CRB2 (تضخم البطين الدماغي مع مرض الكلى الكيسي) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
الملخص التنفيذي: اختبار جيني دقيق بنسبة 99.9% لتشخيص طفرات جين CRB2 المرتبطة بتضخم البطينات الدماغية ومرض الكلى الكيسي باستخدام تقنية التسلسل الجيني من الجيل التالي (NGS)، مع خدمة سحب منزلي معتمدة وتفسير سريري هاتفي بعد النتيجة، ودعم تأميني عبر الواتساب.
Overview
The CRB2 NGS test screens the entire coding region of the CRB2 gene for variants associated with autosomal recessive ventriculomegaly–cystic kidney disease syndrome. في هذا الإطار، يُستخدم التسلسل عالي الإنتاجية للكشف عن الطفرات المسببة للمتلازمة بدقة عالية، مما يدعم التشخيص الدقيق للعائلات المعرضة.
| Feature | Our Test (NGS) | Alternative (Sanger) |
|---|---|---|
| Technology | Next-Generation Sequencing | Single-gene Sanger Sequencing |
| Coverage | Full coding exons ±20 bp splice sites | Limited to targeted exons only |
| Variant Detection | SNVs, indels, CNV clues, novel variants | Known point mutations |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks |
| Price | 2,800 AED | 1,500–2,000 AED (limited scope) |
Physician Insight & Safety Protocol
“As a practicing physician, I advise that this genetic test is a powerful diagnostic tool but must be integrated with your child’s clinical imaging and family history. Genetic findings require careful correlation; not every mutation predicts disease severity, and a negative result does not rule out other genetic aetiologies. Please consult a clinical geneticist for full interpretation.”
— Dr. Prabhakar Reddy (DHA License: 61713011)
⚠️ Medication Warning: Do not discontinue any prescribed medication without consulting your doctor. This test does not replace ongoing clinical management.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Inadequate sample (hemolyzed blood, degraded DNA), known mosaicism requiring tissue analysis.
- ER Red Flags: New-onset seizures, acute loss of consciousness, rapidly rising blood pressure, signs of acute kidney injury (oliguria, edema) — seek emergency care immediately; genetic testing is not for acute diagnosis.
- UAE Regulatory Compliance: This service adheres to Federal Decree-Law No. 41 of 2024, CDS Law 2026 for minors’ data, and UAE PDPL for genetic privacy. ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).
Patient FAQ & Clinical Guidance
1. What is the CRB2 gene ventriculomegaly with cystic kidney disease NGS test?
This test uses Next-Generation Sequencing to analyze the entire CRB2 gene for mutations linked to ventriculomegaly and cystic kidney disease, providing a definitive molecular diagnosis. It is recommended for patients with prenatal ultrasound findings of cerebral ventriculomegaly and renal cysts, or for family screening. Results aid in prognosis, reproductive planning, and specialized care coordination with nephrology and neurology teams. يتم استخدام هذا الاختبار للكشف عن الطفرات الجينية المسببة للمتلازمة.
2. How should I prepare for the test?
You need a blood sample or extracted DNA, and a mandatory genetic counselling session to document a detailed pedigree of affected family members. Fasting is not required; if using an FTA card, a single drop of blood is sufficient. Our home collection team provides all materials. The counselling session ensures proper test selection and informed consent, compliant with UAE PDPL. يُوصى بجلسة استشارة وراثية قبل إجراء الاختبار لرسم شجرة العائلة.
3. Is this covered by insurance in the UAE?
We offer direct billing verification to check your insurance plan’s coverage for genetic testing; simply send your policy details via WhatsApp. Many UAE insurers now include medically indicated genetic tests under hereditary disease benefits. We will assist with pre-authorization and guide you through the process. يُرجى التواصل عبر الواتساب للتحقق من تغطية التأمين للفحص الجيني.
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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All reports reviewed by DHA-Certified physicians