Test Price
2,600 AED✅ Home Collection Available
NxGen Sequencing for Dravet Syndrome & Early Infantile Epileptic Encephalopathy (EIEE) in UAE | 2600 AED | 2026 DHA Guidelines
تحليل التسلسل الجيني من الجيل التالي لمتلازمة درافيت واعتلال الدماغ الصرعي المبكر عند الرضع في الإمارات | 2600 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي
يقدم هذا التحليل الجيني المتطور تشخيصًا دقيقًا بنسبة 99.9% لحالات متلازمة درافيت والاعتلال الدماغي الصرعي المبكر، مع خدمة جمع العينات المنزلية المخصصة وفق معايير الآيزو، وإرشاد طبي فوري بعد النتائج، والتأكيد المباشر للتغطية التأمينية عبر واتساب.
- 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
Test Overview
This NxGen sequencing test screens multiple genes implicated in Dravet syndrome and early infantile epileptic encephalopathies, combining next-generation sequencing (NGS) with confirmatory Sanger sequencing for unparalleled accuracy. In the UAE, the test is processed under ISO 9001:2015 certified facilities, ensuring a 40‑working‑day reporting timeline with rigorous clinical validation. يغطي هذا الاختبار مجموعة شاملة من الجينات المرتبطة بالصرع الطفولي الشديد.
| Parameter | Our NxGen Dravet/EIEE Test | SCN1A Single-Gene Test | Whole Exome Sequencing (WES) |
|---|---|---|---|
| Method | NGS + Sanger Confirmation | Sanger Sequencing | NGS only (with variable interpretability) |
| Genes Analyzed | SCN1A, PCDH19, STXBP1, CDKL5, KCNQ2, ARX, and more (expansive panel) | SCN1A only | All ~20,000 genes (may include incidental findings) |
| Detection of Copy Number Variants | Yes, via NGS depth‑based analysis | Limited | Possible, but often requires additional analysis |
| Turnaround Time | 40 working days | 4–6 weeks | 8–12 weeks |
| Price (AED) | 2600 | ≈1500 | ≈4000 |
Powered by ISO 9001:2015 certified lab (Cert: INT/EGQ/2509DA/3139). Facility License: 9834453.
Physician Insight & Safety Protocol
“As a neurologist with extensive experience in pediatric epilepsy, I understand the anxiety families face when seeking a diagnosis for their child’s seizures. This advanced genetic test can provide the molecular confirmation needed to tailor treatment, but please remember that a positive or negative result must be interpreted in the full clinical context by your physician.”
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & Emergency Red Flags
- Inability to obtain 10 mL venous blood (e.g., severe venous access issues).
- Failure to complete and sign the mandatory Whole Exome Sequencing Consent Form (Form 37).
- Active severe infection with coagulopathy or hemodynamic instability.
🚨 Seek Emergency Care If:
- Prolonged seizure lasting more than 5 minutes or repeated seizures without recovery.
- Respiratory distress, cyanosis, or loss of consciousness.
Patient FAQ & Clinical Guidance
1. What does this NxGen test detect?
This detects pathogenic variants in genes responsible for Dravet syndrome and early infantile epileptic encephalopathies using high-coverage NGS. It covers SCN1A and numerous other genes, identifying point mutations, splice variants, and copy number changes with Sanger‑validated accuracy.
يكشف هذا الاختبار عن الطفرات الجينية المسببة لمتلازمة درافيت واعتلال الدماغ الصرعي المبكر بدقة عالية.
2. How is the sample collected?
A trained phlebotomist collects 10 mL of venous blood in two lavender-top EDTA tubes, refrigerated immediately. Home collection is available 8 AM – 11 PM daily; the sample must be shipped cold (never frozen) and reach our lab by 9 AM for same‑day accessioning.
يتم سحب عينة الدم عبر مختص باستخدام أنابيب الحفظ بالتبريد وترسل بسرعة لضمان الجودة.
3. When will I receive my results?
Results are reported within 40 working days, accompanied by a detailed clinical report. You will also receive a complimentary telephonic guidance session with a genetic counselor or neurologist to explain the findings and next steps.
تصدر النتائج خلال 40 يوم عمل، مع تقرير مفصل واستشارة طبية هاتفية.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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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