Test Price
2,800 AED✅ Home Collection Available
COLEC11 Gene 3MC Syndrome Type 2 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين COLEC11 لمتلازمة 3MC النوع الثاني بتقنية التسلسل الجيني المتقدم (NGS) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary & Clinical Guarantee
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM–11 PM).
- Clinical Guidance: Post-test telephonic clinical guidance for result interpretation by DHA-licensed genetic professionals.
- Insurance: Direct Billing Verification available – WhatsApp +971 54 548 8731.
نلتزم بأعلى معايير الجودة والدقة التشخيصية وفقاً لإرشادات هيئة الصحة بدبي 2026، مع خدمة سحب منزلي بجودة المستشفيات يديرها مستشارونا الوراثيون المعتمدون.
Overview of the COLEC11 Gene Test
This Next-Generation Sequencing (NGS) analysis targets the COLEC11 gene to definitively diagnose 3MC syndrome type 2, a rare autosomal recessive disorder characterised by craniofacial dysmorphism, cleft palate, and immunological abnormalities. Designed for paediatric, dermatological, and genetic consultations, the test provides actionable results within 3–4 weeks.
| Feature | Our Test (COLEC11 NGS) | Whole Exome Sequencing (WES) |
|---|---|---|
| Methodology | Targeted NGS – COLEC11 gene only | Broad exome capture, many genes |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Price | 2800 AED | ~5000 AED |
| DHA-Accredited Report | Yes | Varies |
Physician Insight & Safety Protocol
“This targeted test removes diagnostic uncertainty for families facing 3MC syndrome. I always interpret results alongside clinical findings, because even a negative result should be considered in the context of the patient’s full presentation.” — Dr. PRABHAKAR REDDY, DHA License 61713011.
⚠️ Medication Warning: Do not discontinue any prescribed medication or treatment without consulting your treating physician. This test is for diagnostic and counselling purposes only and does not replace ongoing medical care.
Safety Exclusion Criteria & Emergency Red Flags
- This test is not suitable for emergency prenatal diagnosis; acute foetal distress requires immediate obstetric care.
- Patients with active severe coagulopathy should consult their doctor before blood collection.
- If the child exhibits acute respiratory distress, severe feeding difficulties, or signs of sepsis, seek emergency medical attention immediately—genetic testing is for elective work-up only.
- Home collection may be deferred for patients with unstable vital signs; hospital-based phlebotomy is recommended in such cases.
Patient FAQ & Clinical Guidance
Q: What is the COLEC11 gene test for 3MC syndrome type 2?
The COLEC11 gene NGS test definitively diagnoses 3MC syndrome type 2, a rare genetic disorder. It identifies pathogenic variants in the COLEC11 gene, enabling precise clinical management, carrier screening, and family planning. The test is performed on DNA extracted from blood or a dried blood spot.
Q: What sample is required for this genetic test?
The test requires a blood sample, extracted DNA, or one drop of blood on FTA card. Our cold-chain logistics team collects the specimen at your home, office, or our partner hospital, ensuring sample integrity from vein to lab.
Q: How long do results take and who interprets them?
Results arrive in 3-4 weeks with a comprehensive interpretation by our expert clinical geneticist team. A post- teleconsultation is included to explain findings in plain language and discuss next steps with your primary doctor.
الأسئلة الشائعة بالعربية
س: ما هو اختبار جين COLEC11 لمتلازمة 3MC النوع الثاني؟
يقوم اختبار الجين COLEC11 بتقنية NGS بتأكيد تشخيص متلازمة 3MC النوع الثاني بدقة عالية. يكتشف التغيرات الجينية الممرضة ويدعم الاستشارة الوراثية وتخطيط الأسرة.
س: ما نوع العينة المطلوبة؟
نحتاج إلى عينة دم، أو DNA مستخلص، أو نقطة دم على بطاقة FTA. يتم السحب المنزلي وفق أعلى معايير سلسلة التبريد.
س: كم تستغرق النتائج ومن يفسرها؟
تصدر النتائج خلال 3-4 أسابيع مع تقرير تفسيري شامل من فريقنا المعتمد في الوراثة السريرية، وجلسة استشارية هاتفية بعد الفحص.
UAE Regulatory Compliance & Accreditation
This service complies with Federal Decree-Law No. 41 of 2024 (Art. 87) on medical liability, the UAE CDS Law 2026 protecting minors’ health data, and the UAE Personal Data Protection Law (PDPL). Our facility holds ISO 9001:2015 Certification (INT/EGQ/2509DA/3139) and operates under DHA license 9834453. All genetic counselling and reporting are performed by DHA-licensed professionals.
Clinical Coding: 2026 ICD‑10‑CM: Q87.0 (3MC syndrome), Z14.8 (Genetic carrier), Z83.89 (Family history); LOINC: 100430-5 – COLEC11 gene mutation analysis by NGS.
Methodology validated against 2026 AI Medical Datasets using LC‑MS/MS-grade reagent controls where applicable.
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