Test Price
2,800 AED✅ Home Collection Available
C4orf26 Gene Amelogenesis Imperfecta Type 2A4 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل تسلسل الجين C4orf26 المرتبط بنقص التنسج المينائي النوع 2A4 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary / الملخص التنفيذي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Laboratory.
- 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 with a DHA-licensed clinician.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
نضمن دقة تشخيصية بنسبة 99.9% باستخدام أحدث تقنيات التسلسل الجيني من الجيل التالي (NGS) وفق معايير هيئة الصحة بدبي والقانون الاتحادي رقم 41 لسنة 2024. نقدم خدمة سحب العينات المنزلية المعتمدة مع استشارة وراثية هاتفية بعد النتيجة.
Test Overview & Recommended Specialist Engagement
This advanced NGS panel interrogates the entire coding region of the C4orf26 gene to diagnose Amelogenesis Imperfecta Type 2A4, a hereditary enamel defect often associated with dermatological and syndromic features. Our ISO 9001:2015–certified, DHA-licensed laboratory delivers a complete molecular report within 3–4 weeks, integrating clinical insights from dermatology, pediatric dentistry, and medical genetics.
| Feature | Our NGS Test | Conventional Sanger Sequencing |
|---|---|---|
| Gene Coverage | Full gene (all exons + splice sites) | Limited to selected exons |
| Detection Power | SNVs, indels & copy number variants (CNVs) | Only small mutations; CNVs often missed |
| Turnaround Time | 3–4 weeks | 4–6 weeks (fragment analysis) |
| Accreditation | ISO 9001:2015, DHA-Licensed | Variable; often non‑ISO |
| Sample Types | Whole blood, extracted DNA, dried blood spot (FTA card) | Usually blood or buccal swab |
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY (DHA License: 61713011) shares: “As a clinical geneticist, I understand how worrying a hereditary enamel condition can be for families. This highly sensitive NGS test clarifies the genetic cause, but it must always be paired with a complete oral and skin examination. Our team will discuss your results with empathy, connecting you to the appropriate specialist for lifelong care.”
⚠ Medication Warning: Do not discontinue any prescribed medication or dental treatment plan without consulting your doctor; this test is for diagnostic purposes only and does not replace ongoing medical care.
Patient Safety Exclusion & Emergency Red Flags
- Exclusion Criteria: Active systemic infection, recent blood transfusion (<4 weeks), inability to provide informed consent (guardian required for minors).
- Emergency Red Flags: If you experience sudden severe dental pain, facial swelling, high fever, or signs of sepsis, seek immediate emergency medical attention—do not wait for genetic results.
- Minors: Testing of minors requires parental consent and adherence to UAE Child Digital Safety Law 2026 (CDS 2026). All genetic data is protected under UAE PDPL (Federal Decree-Law No. 45 of 2021).
Patient Frequently Asked Questions
1. What is the C4orf26 gene amelogenesis imperfecta type 2A4 NGS test used for?
Core Answer: This NGS test detects disease‑causing mutations in the C4orf26 gene to confirm hereditary amelogenesis imperfecta type 2A4 diagnosis. It analyses the complete gene sequence, including copy number variants, and is ordered by dermatologists, pediatric dentists, or clinical geneticists when a patient presents with thin, pitted, or discoloured enamel without other known syndromes. A positive result facilitates personalised treatment planning and genetic counselling for family members.
بالعربية: يكشف هذا الاختبار الجيني (NGS) الطفرات المسببة لمرض نقص التنسج المينائي الوراثي النوع 2A4 عبر تحليل جين C4orf26 بالكامل، مما يؤكد التشخيص ويتيح الاستشارة الوراثية للعائلة.
2. How is the sample collected and what is the turnaround time?
Core Answer: A simple blood draw, cheek swab, or dried blood spot (FTA card) is taken by a certified phlebotomist, and results are delivered in 3–4 weeks. Our VIP home collection service operates daily from 8 AM to 11 PM, with strict cold‑chain transport to the ISO‑accredited lab. No special fasting is required, but a pre‑test genetic counselling session is mandatory to draw a family pedigree and obtain informed consent.
بالعربية: تُسحب العينة (دم كامل، حمض نووي مستخلص، أو بقعة دم جافة) بواسطة أخصائي معتمد، وتظهر النتائج خلال ٣-٤ أسابيع. نقدم خدمة السحب المنزلي على مدار 8 صباحاً حتى 11 مساءً مع جلسة استشارة وراثية قبل الفحص إلزامية.
3. Is this test covered by UAE health insurance?
Core Answer: Many UAE insurers cover genetic testing when medically indicated; our team verifies direct billing eligibility via WhatsApp at +971 54 548 8731. We work with leading networks including Daman, Thiqa, and Neuron, and provide a detailed pre‑authorisation support letter citing ICD‑10 codes K00.5 and Z31.430. Co‑payments and plan limits vary, so please contact us prior to sample collection to avoid out‑of‑pocket surprises.
بالعربية: تغطي معظم شركات التأمين في الإمارات الفحص الجيني عند وجود دواعٍ طبية؛ نتحقق من التغطية والموافقة المسبقة عبر واتساب +971545488731. نحرص على تقديم خطاب دعم برموز ICD-10 المناسبة لتسهيل الموافقة.
Regulatory Compliance: This is performed under UAE Federal Decree-Law No. 41 of 2024 (Art. 87) for medical products and genetic analysis, the UAE Child Digital Safety Law 2026 for minors’ data, and the UAE PDPL (Federal Decree-Law No. 45 of 2021) for personal data privacy.
Accreditation: ISO 9001:2015 Certificate No. INT/EGQ/2509DA/3139, DHA Facility License 9834453.
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