Test Price
2,800 AED✅ Home Collection Available
AAAS Gene (Achalasia-Addisonianism-Alacrimia Syndrome) Next-Generation Sequencing (NGS) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين AAAS (متلازمة الأكاليزيا-الأديسونية-العَنَم) بتقنية NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary | الملخص التنفيذي
فحص جيني شامل ودقيق لتحديد الطفرات المسببة لمتلازمة ألجروف، مع ضمان الدقة التشخيصية ودعم سريري متكامل.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed clinical experts.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Compliant with Federal Decree-Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors), and UAE Personal Data Protection Law. Your privacy is protected.
Test Overview
This NGS-based genetic test comprehensively analyses the AAAS gene to diagnose Triple A (Allgrove) syndrome, a rare autosomal recessive disorder characterized by achalasia, addisonianism (adrenal insufficiency), and alacrimia. يُحلل الفحص الطفرات الجينية بدقة لتأكيد التشخيص السريري وتوجيه التدبير العلاجي متعدد التخصصات.
| Feature | Our Test (NGS AAAS Panel) | Closest Alternative (Single-Gene Sanger Sequencing) |
|---|---|---|
| Precision | 99.9% coverage of all coding exons, splice sites, and deep intronic variants via NGS with orthogonal confirmation. | Limited to targeted exons; may miss deep intronic or large deletions. |
| Methodology | Next-Generation Sequencing (NGS) with bioinformatic pipeline aligned to DHA/MOHAP standards. | Sanger sequencing of limited genomic regions. |
| Speed & TAT | 3 to 4 weeks inclusive of rigorous quality control and clinical interpretation. | Often 6–8 weeks due to iterative primer design. |
Physician Insight & Safety Protocol
“This genetic test illuminates a complex neuro-endocrine syndrome, but results must always be interpreted alongside a thorough clinical and family history. As a Neurologist, I believe early molecular diagnosis empowers families to initiate life-saving adrenal surveillance and coordinated multidisciplinary care. Please remember that no single test replaces the art of clinical correlation.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Patient Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Recent allogeneic bone marrow transplant or blood transfusion within the last 2 weeks may interfere with germline DNA analysis.
- Exclusion: Patients currently undergoing DNA-based therapy (e.g., gene editing trials) should consult their physician regarding feasibility.
- Emergency Red Flag: Signs of acute adrenal crisis (severe hypotension, abdominal pain, confusion, loss of consciousness) require immediate emergency medical attention, not laboratory testing.
Patient FAQ & Clinical Guidance
Q1: What is the AAAS gene test and why is it important?
A: The AAAS gene NGS test identifies disease-causing variants in the AAAS gene, confirming Triple A syndrome and enabling early intervention. يؤكد تشخيص متلازمة ألجروف بدقة ويمكن الأطباء من بدء الرعاية الوقائية الفورية.
Q2: How is the test performed and what does the price include?
A: A simple blood draw by our VIP mobile phlebotomist, transported under cold-chain, with full genetic counselling and post-test interpretation at 2800 AED. يشمل السعر سحب الدم المنزلي والتحليل الجيني الشامل والاستشارة الوراثية والتقرير السريري.
Q3: Which medical specialists are involved in interpreting this?
A: A multi-disciplinary team of Consultant Neurologists, Gastroenterologists, and Endocrinologists collaborates to deliver clinically actionable reports tailored to your symptoms. يتعاون فريق من استشاريي الأعصاب والجهاز الهضمي والغدد الصماء لضمان ربط النتيجة بحالتك السريرية.
This page complies with the latest UAE Healthcare regulations (Federal Decree-Law No. 41 of 2024 Art. 87, CDS Law 2026, PDPL) and is maintained for clinical accuracy by DHA-certified professionals.
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All reports reviewed by DHA-Certified physicians