Test Price
2,800 AED✅ Home Collection Available
AUH Gene 3-Methylglutaconic Aciduria Type 1 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين AUH لاعتلال حمض 3-ميثيل غلوتاكونيك من النوع 1 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
ضمان الدقة: حساسية تشخيصية تصل إلى 99.9% عبر معالجة معتمدة وفق معايير ISO.
الخدمات اللوجستية المتميزة: سحب عينات منزلي بمستوى المستشفيات عبر سلسلة تبريد معتمدة ISO، وخدمة الفصادة المتنقلة VIP.
الإرشاد السريري: استشارة هاتفية بعد الفحص لتفسير النتائج سريرياً.
التأمين: التحقق المباشر من التغطية التأمينية عبر واتساب +971 54 548 8731.
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain and VIP Mobile Phlebotomy.
Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview
The AUH Gene NGS test screens for pathogenic variants in the AUH gene to confirm 3-methylglutaconic aciduria type 1, a rare autosomal recessive organic aciduria. This high‑resolution sequencing test provides diagnostic clarity for patients presenting with developmental delay, metabolic acidosis, or family history of the disorder. يُعد تحليل جين AUH بتقنية التسلسل الجيني (NGS) الفحص القياسي لتأكيد اعتلال حمض 3-ميثيل غلوتاكونيك من النوع 1، وهو اضطراب أيضي وراثي نادر.
| Feature | Our NGS Test (Next‑Generation Sequencing) | Closest Alternative (Sanger Sequencing of AUH Gene) |
|---|---|---|
| Precision | >99.9% analytical sensitivity & specificity | High for targeted regions; may miss deep intronic variants |
| Methodology | Full gene sequencing + intron/exon boundaries | Sequences coding exons only |
| Turnaround Time | 3 to 4 Weeks | 3 to 5 Weeks |
| Cost (AED) | 2800 | Variable; often less comprehensive |
Physician Insight & Safety Protocol
“As a clinician with extensive experience in metabolic genetics, I emphasize that this NGS panel is a powerful diagnostic tool, yet results must be correlated with clinical presentation and biochemical markers. A positive test confirms the genetic diagnosis but does not predict individual disease trajectory, and I strongly recommend pre‑ and post‑test genetic counselling to interpret implications for the patient and their family.” — Dr. Prabhakar Reddy, DHA License: 61713011
⚠️ Do not discontinue prescribed medication or supplements without consulting your treating physician. Genetic test results are not a substitute for ongoing clinical management.
Safety & Exclusion Criteria
- Minors: Genetic testing for minors requires documented consent from a legal guardian and a genetic counselling session (CDS Law 2026).
- Informed Consent: A signed informed consent form is mandatory; individuals unable to understand the implications should be assisted by an authorized representative.
- Sample Suitability: Hemolyzed, clotted, or mislabelled specimens will be rejected. Ensure whole blood is collected in EDTA tubes.
- Acute Illness: Testing should be deferred in cases of severe intercurrent infection or metabolic crisis unless specifically indicated by the attending physician.
- ⚠️ ER Red Flags: If you or your child experience sudden lethargy, vomiting, seizures, or loss of consciousness, seek immediate emergency medical care. These symptoms could indicate a metabolic decompensation unrelated to the test procedure.
Frequently Asked Questions
1. What is the AUH gene test for 3-methylglutaconic aciduria type 1?
This Genetic Test sequences the entire AUH gene to detect pathogenic variants responsible for 3-methylglutaconic aciduria type 1, aiding in diagnosis, family planning, and management. يقوم هذا الاختبار الجيني بتقنية التسلسل الكامل لجين AUH للكشف عن الطفرات المسببة لاعتلال حمض 3-ميثيل غلوتاكونيك من النوع 1، مما يساعد في التشخيص والتخطيط الأسري وإدارة المرض.
2. How should I prepare for the, and what sample is required?
No fasting is needed; a blood sample (one tube of EDTA whole blood) or a drop of blood on an FTA card is collected by our certified phlebotomist during the home visit. لا حاجة للصيام؛ يتم أخذ عينة دم (أنبوب واحد من الدم الكامل المحتوي على مانع التخثر EDTA) أو قطرة دم على بطاقة FTA بواسطة أخصائي سحب الدم المعتمد خلال الزيارة المنزلية.
3. How long does it take to receive results, and how are they delivered?
Results are typically ready in 3 to 4 weeks and are delivered through a secure electronic report; a follow-up tele‑consultation with a genetic counsellor is included. تكون النتائج جاهزة عادةً خلال 3 إلى 4 أسابيع، وتُسلّم عبر تقرير إلكتروني آمن، مع استشارة هاتفية متابعة مع مستشار وراثي.
This service is provided by a DHA-licensed facility (License: 9834453). All genetic data is processed in accordance with UAE Federal Decree-Law No. 41 of 2024 and the UAE Personal Data Protection Law. Not intended for diagnostic use in isolation; clinical correlation is essential. Contact us for support: +971545488731 (WhatsApp).
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