Test Price
2,800 AED✅ Home Collection Available
ERCC2 Gene Trichothiodystrophy Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين ERCC2 لمتلازمة ترايكوثيوديستروفى في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited Next‑Generation Sequencing — results you can trust.
Premium Logistics: Paid Hospital‑Grade Home Collection via ISO Certified Cold‑Chain Home Collection & VIP Mobile Phlebotomy (8 AM–11 PM).
Clinical Guidance: Telephonic Post‑Test Clinical Guidance to interpret your results with a DHA‑licensed specialist.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
فحص وراثي دقيق لتشخيص متلازمة ترايكوثيوديستروفى عبر تقنية التسلسل الجيني المتطور، بأعلى معايير الجودة والخدمة المنزلية الفورية.
Test Overview & Methodology Comparison
The ERCC2 Gene Trichothiodystrophy NGS Test is a comprehensive DNA‑based analysis that screens for pathogenic variants in the ERCC2 gene, confirming or ruling out trichothiodystrophy (TTD). هذا الفحص الجيني الشامل يؤكد أو يستبعد متلازمة ترايكوثيوديستروفى عبر تحليل طفرات جين ERCC2.
| Feature | Our Test (ERCC2 NGS) | Closest Alternative (Single‑Gene Sanger) |
|---|---|---|
| Precision | 99.9% analytical sensitivity via NGS; full coding region ± splice sites | Limited to pre‑selected exon(s); may miss deep intronic or large deletions |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks |
| Suitable Samples | Whole Blood, Extracted DNA, Dried Blood Spot (FTA Card) | Whole Blood only |
| Price | 2800 AED | ~3500 AED |
| Clinical Utility | Covers all known TTD‑associated variants; supports family screening & cancer surveillance | Often requires sequential testing if first exon is negative |
Clinical Advisory & Safety Protocol
Dr. Prabhakar Reddy (DHA License: 61713011) notes:
“Every ERCC2 result must be correlated with a thorough dermatological and neurological examination. A positive finding confirms the genetic basis of trichothiodystrophy but does not define its severity; clinical follow‑up is essential. I strongly advise patients to share all results with their managing physician before altering any care plan.”
Medication Warning:
Do not discontinue prescribed medication without consulting your doctor. This test is diagnostic; treatment adjustments should only be made under specialist guidance.
Safety Exclusion Criteria & ER Red Flags
- If the patient develops acute severe sunburn‑like skin blistering or rapid neurological decline, seek emergency medical care immediately — this test is not a substitute for acute management.
- Collection cannot proceed if the patient is unable to provide informed consent or has a bleeding disorder that makes phlebotomy unsafe (discuss with our clinical team).
- Neonates: a minimum weight of 2.5 kg is required for venous sampling; an FTA heel‑prick card may be used instead.
- Recent bone marrow transplant or blood transfusion within 30 days may interfere with germline genetic analysis; please inform the laboratory.
Patient FAQ & Clinical Guidance
What is the ERCC2 gene test, and who should consider it?
This test detects DNA changes in the ERCC2 gene that cause trichothiodystrophy, a rare condition affecting hair, skin, and often the nervous system. It is recommended for individuals with sulfur‑deficient brittle hair, ichthyosis, photosensitivity, or a family history of TTD. Referral from a dermatologist, clinical geneticist, or oncologist is advised, especially when cancer predisposition (xeroderma pigmentosum‑TTD overlap) is suspected.
يكتشف هذا الفحص التغيرات الجينية في جين ERCC2 المسؤولة عن متلازمة ترايكوثيوديستروفى، ويُوصى به لمن يعانون من شعر هشّ فقير بالكبريت أو حساسية جلدية للضوء أو تاريخ عائلي. ننصح بالإحالة من طبيب أمراض جلدية أو مختص في الوراثة السريرية.
How is the sample collected, and how long until I receive the report?
A certified phlebotomist collects one small blood sample (or a dried spot) at your home within 60 minutes, and your full NGS report is ready in 3–4 weeks. We accept whole blood in EDTA tubes, extracted DNA, or a simple FTA card. The sample is transported under strict cold‑chain protocols to our ISO‑accredited laboratory. Once sequencing is complete, the report is reviewed by a molecular geneticist and returned with a telephonic consultation option.
يُسحب عينة دم صغيرة في المنزل بواسطة مختص معتمد خلال 60 دقيقة، وتصدر النتيجة الشاملة خلال 3–4 أسابيع. تُنقل العينة تحت ظروف تبريد صارمة إلى مختبرنا المعتمد دوليًا، ويُراجع التقرير أخصائي جينات قبل التسليم مع استشارة هاتفية.
Will my insurance cover the 2800 AED cost, and how do I book?
We offer direct billing verification with all major UAE insurers—simply send your Emirates ID and insurance card via WhatsApp to +971 54 548 8731. If self‑pay, you receive an official invoice for reimbursement. Booking is immediate: our patient coordinator confirms your home collection slot (8 AM–11 PM) and ensures you complete the mandatory pre‑ genetic counseling. No hidden fees; the 2800 AED covers the entire process from consent to clinical guidance.
نتحقق من تغطية التأمين مباشرة عبر واتساب على الرقم 971545488731، ونقدّم فاتورة رسمية للاسترداد إذا كنت تدفع نقدًا. احجز موعد السحب المنزلي فورًا، وتأكد من إكمال جلسة الاستشارة الوراثية اللازمة قبل الفحص؛ 2800 درهم تغطي كامل الخدمة بلا رسوم إضافية.
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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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ISMS 27001:2022
ISO Accredited
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All reports reviewed by DHA-Certified physicians