Test Price
2,800 AED✅ Home Collection Available
FAM20A Gene Amelogenesis Imperfecta Type 1G Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين FAM20A وخلل تنسج الميناء النوع 1G في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
✅ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Certified Next-Generation Sequencing (NGS) with Sanger Confirmation at our CAP-Accredited Laboratory.
🚑 Premium Logistics: Complimentary Hospital-Grade Home Collection by DHA-Licensed Phlebotomists (8 AM – 11 PM) with ISO-Certified Cold-Chain Transport.
📞 Clinical Guidance: Post-Test Telephonic Interpretation by a Clinical Geneticist included in the 2800 AED fee.
📋 Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731 (all major UAE insurers accepted).
هذا التحليل الجيني المعتمد من هيئة الصحة بدبي يوفر تشخيصًا دقيقًا لخلل تنسج الميناء من النوع 1G المرتبط بطفرات جين FAM20A، مع الالتزام الكامل بالقانون الاتحادي رقم 41 لسنة 2024 وقانون حماية البيانات الشخصية في الإمارات.
Overview
The FAM20A Gene Amelogenesis Imperfecta Type 1G Genetic Test analyzes the entire coding region of the FAM20A gene to detect pathogenic variants causing autosomal recessive Amelogenesis Imperfecta Type IG (enamel-renal syndrome or gingival hyperplasia syndrome). This test, available at 2800 AED with a 3–4 week turnaround, uses next-generation sequencing and Sanger validation for 99.9% diagnostic accuracy. بالعربية: يقوم التحليل بفحص شامل لجين FAM20A لتشخيص خلل تنسج الميناء الوراثي.
| Feature | Our Test: FAM20A Targeted NGS | Closest Alternative: Whole Exome Sequencing (WES) |
|---|---|---|
| Precision | >99% sensitivity for FAM20A variants; deep coverage (>100×) | ~95% sensitivity for FAM20A; coverage may be uneven |
| Method | NGS + Sanger confirmation of all detected variants | WES + optional Sanger (additional cost) |
| Speed | 3–4 Weeks | 6–8 Weeks |
| Cost in UAE | 2800 AED (all-inclusive) | 5000–8500 AED |
| Clinical Focus | Dental enamel defect + renal/gum syndromes | Broad: may miss single-gene focus |
Physician Insight & Safety Protocol
“As a Clinical Geneticist, I emphasize that a positive FAM20A result must be correlated with clinical dental and renal findings. Genetic counseling is critical for families, as this condition follows autosomal recessive inheritance. This test provides the molecular confirmation necessary for precise reproductive planning and early intervention.”
— Dr. PRABHAKAR REDDY, DHA License 61713011, Consultant Geneticist
⚠️ Do not discontinue any prescribed medications or dental treatments without first consulting your specialist.
Patient Safety: Exclusion Criteria & Red Flags
- Exclusion: Patients unable to provide informed consent, those with acute febrile illness (postpone blood draw), or those with severe anemia (Hb < 8 g/dL) – home collection may need a medical facility visit.
- Exclusion: Genetic testing of a minor requires a DHA-approved genetic counsellor’s written consent and, where applicable, parental agreement per UAE Child Rights Law.
- ER Red Flag: If you experience sudden dental pain, facial swelling, or signs of renal colic (severe flank pain), seek immediate medical attention – not related to the test but to possible syndrome complications.
Patient FAQ & Clinical Guidance
1. What does the FAM20A gene test detect, and who should consider it?
Snippet: This test identifies mutations in the FAM20A gene linked to enamel defects and kidney calcifications.
It is recommended for individuals with thin or pitted enamel, early tooth loss, gum overgrowth, or a family history of Amelogenesis Imperfecta, especially when renal symptoms are present. Ideal candidates include children (with proper consent), adults planning a family, and those with unexplained dental anomalies.
يكشف هذا التحليل الطفرات في جين FAM20A المرتبطة بعيوب الميناء وتكلسات الكلى. يُنصح به لمن لديهم أسنان رقيقة أو منقّرة، أو تضخم اللثة، أو تاريخ عائلي للمرض.
2. How is the test performed and when will I receive results?
Snippet: A simple blood draw or FTA card sample is collected at home, with results in 3–4 weeks.
Our DHA-licensed phlebotomist will visit your location (8 AM–11 PM, 7 days a week). No fasting is required. The sample is transported in a temperature-controlled kit to our ISO 15189-accredited lab. After sequencing, a detailed report with clinical interpretation will be shared via secure portal, and a genetic counsellor will call to explain the findings.
يتم سحب عينة دم بسيطة في المنزل، وتظهر النتائج خلال 3–4 أسابيع. لا حاجة للصيام، ويتم النقل وفق معايير سلسلة التبريد المعتمدة.
3. Is this test covered by UAE health insurance?
Snippet: Most UAE insurers cover genetically indicated tests like FAM20A when pre-authorised by a Dermatologist or Geneticist.
We provide direct billing verification. Simply WhatsApp your Emirates ID and insurance card to +971 54 548 8731. Our team will confirm coverage within 2 hours. If the is not fully covered, you can opt for the 2800 AED self-pay rate, which includes all services.
معظم شركات التأمين في الإمارات تغطي هذا التحليل الجيني عند وجود إحالة من طبيب مختص. نقدم خدمة التحقق المباشر من التغطية عبر واتساب.
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