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4,000 AED

✅ Home Collection Available

AAAS Full Gene Sequence Analysis (Allogrove Syndrome) in UAE | 4000 AED | 2026 DHA Guidelines

تحليل تسلسل جين AAAS الكامل (متلازمة ألغروف) في الإمارات | 4000 درهم | معتمد من هيئة الصحة بدبي

Definitive Molecular Diagnosis | 99.9% Diagnostic Sensitivity | Sanger Sequencing Gold Standard | Home Collection 8 AM – 11 PM

🇦🇪 UAE Clinical Excellence & Patient-First Service

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Laboratory (Cert: INT/EGQ/2509DA/3139).
  • Premium Logistics: Hospital-Grade Home Collection with ISO-Certified Cold-Chain Transport.
  • Clinical Guidance: Complimentary Post-Test Telephonic Interpretation by a licensed clinician.
  • Insurance Support: Direct Billing Verification via WhatsApp +971 54 548 8731 (MOHAP compliant).

ضمان دقة تشخيصية بنسبة 99.9% من خلال مختبر معتمد آيزو 9001:2015.

خدمة سحب منزلي بمستوى المستشفى ونقل مبرد معتمد دوليًا (السلسلة الباردة).

استشارة طبية هاتفية مجانية بعد النتيجة لتفسيرها.

تحقق مباشر من تغطية التأمين عبر واتساب: +971545488731.

Test Overview

This full gene sequence analysis employs Sanger sequencing to interrogate the entire coding region and splice junctions of the AAAS gene, providing a definitive molecular diagnosis of Allogrove (Triple A) Syndrome with 99.9% sensitivity. تحليل شامل لتسلسل جين AAAS بواسطة تقنية سانجر لتشخيص متلازمة ألغروف بدقة متناهية.

Feature Our AAAS Full Gene Sequence Analysis Closest Alternative (NGS Panel)
MethodologyBidirectional Sanger Sequencing (Gold Standard)Next-Generation Sequencing (Targeted Panel)
CoverageEntire gene, including deep intronic/exonic boundariesLimited to selected exons; may miss rare variants
Turnaround Time2-3 Weeks2-4 Weeks
Clinical Confidence99.9% Diagnostic Sensitivity~85-95% for known variants

Physician Insight & Safety Protocol

“As a gynecologist with focus on maternal-fetal medicine, I stress that every genetic result must be interpreted in the context of full clinical and family history. This Sanger-based test offers unmatched precision, but it complements—never replaces—thorough clinical evaluation. Early diagnosis empowers families to plan proactive, multidisciplinary care.”

— Dr. PRABHAKAR REDDY, Senior Consultant, DHA License: 61713011

‼ Medication Warning:

Do not discontinue prescribed medication or alter treatment plans based solely on this test result without consulting your managing physician.

Exclusion Criteria & ER Red Flags: Invasive prenatal sampling (amniocentesis/CVS) must be performed by a qualified specialist in a licensed facility after thorough counseling. Seek emergency care immediately if you experience fever, severe abdominal pain, fluid leakage, or bleeding after any invasive procedure. For peripheral blood collection, risks are minimal but stop pressure if hematoma expands.

Patient FAQ & Clinical Guidance

1. What is the AAAS Full Gene Sequence Analysis?

This diagnostic sequences the entire AAAS gene to detect mutations responsible for Allogrove Syndrome, a rare autosomal recessive disorder affecting the adrenal glands, esophagus, and tear production.

فحص تسلسل كامل لجين AAAS يكشف الطفرات المسببة لمتلازمة ألغروف، وهو اضطراب وراثي نادر يؤثر على الغدد الكظرية والمريء وإفراز الدموع.

2. How is the sample collected, and is home collection available?

Samples are obtained via a simple blood draw, or for prenatal cases, amniotic fluid, chorionic villi, or cord blood may be used under strict medical supervision. Our ISO-certified VIP phlebotomy team provides paid home collection between 8 AM and 11 PM across the UAE.

يتم جمع العينة بسحب دم بسيط، أو عبر السائل الأمنيوسي أو الزغابات المشيمية أو دم الحبل السري للحوامل تحت إشراف طبي. نوفر خدمة سحب منزلي مدفوعة ومعتمدة من 8 صباحًا حتى 11 مساءً.

3. How long does it take to receive results, and how will I understand them?

Results are typically ready within 2-3 weeks. You will receive a secure electronic report, followed by a complimentary teleconsultation with a clinician who will explain the findings in plain language and outline next steps.

تصدر النتائج خلال 2-3 أسابيع. بعدها تحصل على استشارة هاتفية مجانية مع طبيب مختص لشرح النتائج وتوجيهك للخطوات التالية.

Methodology: Sanger Sequencing (CE-IVD validated) | LOINC 93307-9 | ICD-10-CM: Q87.8, E25.8, Z13.79 | Facility License: 9834453 | ISO 9001:2015 Cert: INT/EGQ/2509DA/3139

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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.

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