Test Price
2,800 AED✅ Home Collection Available
CNOT3 Gene Cardiac Defects Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CNOT3 للكشف عن عيوب القلب الخلقية عبر تقنية التسلسل الجيني من الجيل التالي (NGS) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
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: Telephonic Post-Test Clinical Guidance in result interpretation by DHA‑licensed physicians.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
يُقدم هذا التحليل الجيني الشامل ضمان دقة تشخيصية تصل إلى 99.9% وفقًا لمعايير هيئة الصحة بدبي لعام 2026.
Test Overview & Comparison
This CNOT3 NGS test comprehensively evaluates the entire coding region of the CNOT3 gene for pathogenic variants causing congenital heart defects. يفحص هذا الفحص الجيني الشامل جين CNOT3 بحثًا عن الطفرات المسببة لعيوب القلب الخلقية. It is the most advanced next-generation sequencing method available in the UAE.
| Feature | Our CNOT3 NGS Test | Conventional Sanger Sequencing |
|---|---|---|
| Precision | 99.9% sensitivity; detects SNVs, indels, CNVs | ~95% for point mutations; misses large rearrangements |
| Methodology | NGS (Illumina® platform) with 100x coverage | Bidirectional Sanger of individual exons |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks (for full gene) |
Physician Insight & Safety Protocol
“As a cardiologist, I understand the worry that comes with genetic testing for heart conditions. This CNOT3 NGS assay provides high-resolution molecular data, but every result must be correlated with your child’s clinical picture and family history. Please do not make any treatment changes without consulting your physician.” — Dr. PRABHAKAR REDDY, DHA License: 61713011
Safety Exclusion Criteria & ER Red Flags
- Exclusion: Recent blood transfusion (≤ 2 weeks), active systemic infection, bone marrow transplant within 6 months.
- ER Red Flags: Seek immediate medical attention if you or your child experiences sudden chest pain, bluish skin (cyanosis), severe shortness of breath, or fainting.
Patient FAQ & Clinical Guidance
Q: What is the CNOT3 Genetic Test?
CNOT3 next-generation sequencing identifies mutations in CNOT3 gene causing congenital heart defects with high accuracy.
This test analyses the entire CNOT3 gene using Illumina NGS technology, detecting single nucleotide variants, small insertions/deletions, and copy number changes. It is the definitive molecular tool for diagnosing CNOT3-related cardiac malformations such as atrial septal defects, ventricular septal defects, and tetralogy of Fallot.
يُحدد تسلسل الجيل التالي لجين CNOT3 الطفرات المسببة لعيوب القلب الخلقية بدقة عالية.
يقوم هذا الفحص بتحليل كامل جين CNOT3 بحثاً عن التغيرات الجينية المرتبطة بتشوهات القلب الخلقية.
Q: Who should consider this test?
Patients with congenital heart defects or family history of CNOT3-related anomalies should undergo this NGS test.
Ideal candidates include newborns, children, and adults with unexplained congenital heart disease, as well as parents planning future pregnancies after a previous affected child. Pre-test genetic counselling is mandatory to interpret results accurately and to draw a family pedigree.
يجب على المرضى الذين يعانون من عيوب خلقية في القلب أو تاريخ عائلي لاضطرابات مرتبطة بـ CNOT3 إجراء هذا الفحص الجيني.
Q: What is the testing process and turnaround time?
Home blood collection is performed by a certified nurse; results take 3–4 weeks using NGS.
A small blood sample (or one drop on an FTA card) is collected in the comfort of your home under ISO‑certified cold‑chain protocols. The sample is shipped to our CAP‑accredited Genetic consultation with a cardiologist-geneticist team.
يتم سحب عينة الدم في المنزل بواسطة ممرض معتمد؛ وتظهر النتائج خلال 3–4 أسابيع باستخدام تقنية NGS.
For appointments or insurance verification, WhatsApp +971 54 548 8731 (Licensed Facility: 9834453). All services comply with Federal Decree‑Law No. 41 of 2024 (Art. 87), UAE Child Data Safety Law 2026, and UAE PDPL.
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