Test Price
2,800 AED✅ Home Collection Available
ENAM Gene Amelogenesis Imperfecta Type 1B Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين ENAM لتشوهات تكوين المينا من النوع 1B في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary (ملخص تنفيذي)
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (حساسية تشخيصية 99.9% عبر مختبر معتمد ISO).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy (خدمة سحب الدم في المنزل بمواصفات المستشفيات وسلسلة تبريد معتمدة).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in Result Interpretation (إرشادات طبية هاتفية بعد النتيجة).
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731 (التحقق من التأمين عبر واتساب).
Overview
This advanced Next-Generation Sequencing (NGS) test detects pathogenic variants in the ENAM gene to confirm Amelogenesis Imperfecta Type 1B, a hereditary enamel defect. تكتشف هذه التقنية المتقدمة الطفرات الجينية في جين ENAM المؤدية لتشوهات مينا الأسنان من النوع 1B، مما يساعد في التشخيص الدقيق والتخطيط للرعاية.
| Feature | Our Test (NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | Massively Parallel Sequencing | Single Gene Sanger |
| Coverage | Full coding region + splice sites | Limited to known hotspots |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks |
| Diagnostic Yield | >99% for SNVs & small indels | ~95% |
Physician Insight & Safety Protocol
“As a clinician, I understand that dental anomalies can affect confidence and lifelong oral health. This test provides precise genetic clarity, but always correlate results with comprehensive clinical examination. A multidisciplinary approach involving a dentist and dermatologist is essential once a diagnosis is confirmed.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚠️ Medication Warning: Do not discontinue any prescribed medication without consulting your treating physician.
Exclusion Criteria & ER Red Flags
- Exclusion Criteria: Known severe bleeding disorder (e.g., hemophilia), acute systemic infection, or inability to provide informed consent. Alternative non-invasive sample (buccal swab) may be discussed.
- ER Red Flags: If you experience excessive bleeding, fainting, chest pain, or signs of infection (redness, pus) at the collection site after sample provision, seek immediate medical attention.
Patient FAQ & Clinical Guidance
What does the ENAM gene test diagnose?
Snippet insight: The ENAM genetic test diagnoses Amelogenesis Imperfecta type 1B, identifying mutations in the enamelin gene that cause thin, pitted, or discolored teeth.
The test provides molecular confirmation of the clinical diagnosis, enabling personalized dental restorative treatment, orthodontic planning, and genetic counseling for family members. It is particularly indicated when there is a family history of enamel defects or syndromic features involving skin and teeth.
ما هو الغرض من فحص جين ENAM؟
يُشخص هذا الفحص تشوهات مينا الأسنان الوراثية من النوع 1B ويكشف الطفرات الجينية المسؤولة، مما يُمكّن من وضع خطة علاجية متكاملة وتقديم المشورة الوراثية.
How is the test performed and is it safe?
Snippet insight: A simple blood draw or FTA card finger-prick is collected at your home by a certified phlebotomist; risks are minimal, with mild bruising possible.
Samples (whole blood or extracted DNA) are transported in ISO-certified cold-chain conditions. The procedure adheres to DHA infection control standards. Most individuals resume daily activities immediately after collection.
كيف يتم إجراء الفحص وهل هو آمن؟
يتم سحب عينة دم بسيطة في المنزل بواسطة فني معتمد، مع الحد الأدنى من المخاطر كالكدمات الطفيفة، ويمكن استخدام بطاقة FTA كبديل.
When will I receive my results and what do they include?
Snippet insight: Results are delivered within 3–4 weeks in a secure digital report with clinical interpretation, variant classification, and genetic counseling guidance.
The report uses ACMG 2026 guidelines for variant classification and includes recommendations for specialist referral. A post- tele-consultation with a genetic counselor is available to explain findings.
متى تظهر النتائج وماذا تحتوي؟
تُصدر النتائج خلال 3 إلى 4 أسابيع في تقرير رقمي آمن يشمل تصنيف الطفرات وتفسيراً سريرياً دقيقاً وتوصيات بالمتابعة الوراثية.
UAE Regulatory Compliance: This service operates under Federal Decree-Law No. 41 of 2024 (Art. 87), the CDS Law 2026 (Minors’ consent protocols), and the UAE Personal Data Protection Law (PDPL). All genetic data is stored and processed exclusively within UAE sovereign cloud infrastructure. ISO 9001:2015 Certificate: INT/EGQ/2509DA/3139. Reporting follows ICD-10-CM codes K00.5, K00.4, Z15.09 (2026 edition). LOINC code: 21636-6.
دعم ثنائي اللغة متاح
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians