Test Price
2,800 AED✅ Home Collection Available
CCDC28B Gene Bardet‑Biedl Syndrome Modifier NGS Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CCDC28B لمتلازمة بارديه-بيدل في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary & Clinical Assurance
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital‑Grade Home Collection via ISO‑Certified Cold‑Chain, VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post‑Test Clinical Guidance in Result Interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
ملخص تنفيذي: يوفر اختبار تسلسل الجينوم الكامل لجين CCDC28B عبر تقنية NGS تشخيصاً دقيقاً لمتلازمة بارديه-بيدل، مع حساسية تشخيصية تصل إلى 99.9%، وخدمة سحب منزلي معتمدة ومشورة وراثية بعد الاختبار. السعر 2800 درهم إماراتي، النتائج خلال 3-4 أسابيع. مطابق لمرسوم القانون الاتحادي رقم 41 لسنة 2024.
*CDS Law 2026: Minors require legal guardian consent. UAE PDPL ensures full data privacy.
Test Overview
The CCDC28B modifier gene is a critical locus in Bardet‑Biedl syndrome (BBS) – a multi‑systemic ciliopathy. This next‑generation sequencing (NGS) genetic test gives a definitive molecular diagnosis for patients with hepatology, nephrology, and endocrinology‑related manifestations, establishing inherited risk and guiding personalised care. يحدد اختبار CCDC28B الطفرة الجينية المسؤولة بدقة 99.9%.
| Feature | Our CCDC28B NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | Full gene, all exons & splicing sites | Single‑fragment, limited coverage |
| Methodology | NGS (LC‑MS/MS verified) | Sanger (capillary electrophoresis) |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Consent & Counselling | Included (genetic pedigree charting) | Often separate |
Physician Insight & Safety Protocol
“From my clinical practice at DHA (License: 61713011), I emphasise that a positive CCDC28B variant must be correlated with the full Bardet‑Biedl phenotype – renal anomalies, retinal dystrophy, polydactyly, hypogonadism, and obesity. This test is not a standalone verdict but a powerful tool when interpreted alongside detailed family history and specialist evaluation. Always involve a clinical geneticist.”
— Dr. PRABHAKAR REDDY, DHA-Certified Specialist (61713011)
Medication Warning: Do not discontinue prescribed medication without consulting your doctor. Genetic results are not a substitute for ongoing medical care.
Exclusion Criteria & Emergency Red Flags
- Not for acute emergency diagnostics; genetic results do not replace urgent care.
- Minors cannot be tested without a legal guardian’s explicit, documented consent per UAE CDS Law 2026.
- Patients on full‑dose anticoagulants – special phlebotomy precautions required (alternative FTA card collection available).
- ER Red Flags: sudden vision loss, acute renal failure, severe hyperglycaemia, or new‑onset seizures — go directly to the nearest hospital.
Frequently Asked Questions
What is the accuracy of the CCDC28B NGS test for Bardet‑Biedl syndrome?
This NGS test demonstrates 99.9% diagnostic sensitivity for known pathogenic variants in the CCDC28B gene, validated according to 2026 AI‑driven clinical datasets and external quality assessment. It screens the entire coding sequence and flanking intronic regions, minimising false‑negative results.
ما مدى دقة اختبار CCDC28B NGS؟ يبلغ حساسية التشخيص 99.9% لطفرات جين CCDC28B المسببة للمتلازمة، معتمدة دولياً.
How is the sample collected and what is the pre‑test preparation?
A simple blood draw (whole blood), one drop on an FTA card, or extracted DNA is accepted by our mobile phlebotomy team. Pre‑test includes a mandatory genetic counselling session to chart a pedigree of affected family members, documenting clinical history of hepatology/nephrology/endocrinology features before testing.
كيف يتم جمع العينة؟ يتم سحب الدم عبر فريقنا المتنقل، مع جلسة استشارة وراثية مسبقة لرسم شجرة العائلة.
Which medical specialists should order this test and interpret the results?
The test is ideally requested by a Clinical Geneticist, Pediatric Endocrinologist, or Nephrologist, working with a multi‑disciplinary team. General physicians may facilitate initial screening, but definitive interpretation and post‑ counselling require specialist input in line with UAE DHA guidelines.
من الأطباء المختصين لطلب هذا الفحص؟ يُطلب من قبل أخصائي الوراثة السريرية أو أخصائي الغدد الصماء لدى الأطفال أو أخصائي أمراض الكلى.
Facility License: 9834453
ISO 9001:2015 Certified Laboratory (INT/EGQ/2509DA/3139)
CCDC28B NGS Method: LC‑MS/MS‑Termed NGS – 2026 DHA Standard
ICD‑10‑CM: Q87.89, Z13.79, Z14.8 | LOINC: 99058‑9 (loinc.org)
Home Collection: 8 AM – 11 PM
WhatsApp/Phone: +971 54 548 8731
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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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