Test Price
2,800 AED✅ Home Collection Available
ATIC Gene AICA-Ribosiduria due to ATIC Deficiency Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين ATIC لعوز إنزيم AICA-ريبوسيدوريا في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Guaranteed Diagnostic Precision with UAE-Compliant, E-E-A-T Driven Care
فحص جيني متقدم عبر تقنية التسلسل من الجيل التالي، يوفر دقة تصل إلى 99.9% بتوصيل عينات منزلي معتمد آيزو، مع إرشاد سريري ما بعد التحليل من قبل أطباء مرخصين من هيئة الصحة بدبي، وبأسعار شفافة تبلغ 2800 درهم. نتائج موثوقة خلال 3 إلى 4 أسابيع.
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Laboratory Operations.
- ✓ Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- ✓ Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed physicians.
- ✓ Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731 (UAE Insurance Coverage Pre-approval).
Comprehensive ATIC Deficiency Analysis: Overview
The ATIC Gene Genetic Test detects pathogenic variants in the ATIC gene causing AICA-ribosiduria, a severe autosomal recessive disorder of purine metabolism. This test screens the entire coding region via Next Generation Sequencing, providing definitive diagnosis and carrier status for affected families in the UAE. بالتوازي مع ذلك، يوفر هذا التحليل الجيني الشامل رؤية متكاملة للطفرات الوراثية المسببة للمرض، مما يدعم اتخاذ القرارات الطبية الوقائية والعلاجية بدقة عالية.
| Feature | Our ATIC NGS Test (UAE) | Conventional Single‑Gene Sequencing |
|---|---|---|
| Precision | >99.9% analytical sensitivity with full exon coverage | ~95% due to limited read depth and incomplete regions |
| Methodology | Illumina NGS with Sanger confirmation for clinically significant variants | Capillary sequencing of selected exons, often missing deep intronic mutations |
| Turnaround Time | 3–4 Weeks (including expert interpretation) | 6–8 Weeks, slower due to fragmented workflow |
| Clinical Interpretability | DHA/MOHAP‑standard nomenclature and ACMG‑classified variant reporting | Often generic reports without correlation to UAE population databases |
Physician Insight & Safety Protocol
“As a DHA-licensed clinical geneticist, I emphasize that a positive ATIC result is not a solitary diagnostic verdict but must be integrated into a thorough clinical and biochemical evaluation. This test is a powerful tool, yet it is the correlation with a patient’s symptoms, family history and amino-imidazole carboxamide measurements that truly guides management. At our center, we ensure every result is discussed with the ordering physician and patient to chart a safe, personalised care pathway.”
— Dr. PRABHAKAR REDDY (DHA License: 61713011), Lead Molecular Geneticist & Internal Medicine Consultant
⚠ Medication Warning
Do not discontinue any prescribed medication or supplement without consulting your doctor. Genetic test results may influence treatment strategies, but sudden cessation can be dangerous.
Exclusion Criteria & Emergency Red Flags:
- Individuals unable to provide informed consent (unless legally authorized representative available).
- Active severe infection or acute metabolic decompensation requiring immediate hospitalization—seek emergency care first.
- Recent blood transfusion (<2 weeks) may cause sample contamination; reschedule as advised.
- If the patient experiences seizures, severe vomiting, lethargy, or loss of consciousness, proceed to the nearest emergency department immediately.
Patient FAQ & Clinical Guidance
What does the ATIC NGS test detect and how long will I wait for results?
The test screens the entire coding sequence of the ATIC gene for disease-causing variants linked to AICA-ribosiduria, a rare metabolic disorder, providing near‑definitive diagnosis within 3 to 4 weeks.
يكتشف فحص جين ATIC جميع الطفرات الممرضة المسؤولة عن متلازمة عوز AICA-ريبوسيدوريا، ويتم تقديم النتائج الشاملة خلال 3 إلى 4 أسابيع.
Can this test be used for a healthy individual wanting a genetic check before marriage in the UAE?
Yes, as a carrier screening test, it aligns with the UAE’s premarital genetic screening guidelines under Federal Decree‑Law No. 41 of 2024, helping couples understand the risk of having an affected child.
نعم، يمكن استخدامه كفحص للأزواج المقبلين على الزواج، وفقاً للقوانين الإتحادية الإماراتية وبروتوكولات هيئة الصحة بدبي، لتقييم خطر إنجاب أطفال مصابين بالمرض.
How does home collection work and what are the sample requirements?
A DHA-certified mobile phlebotomist arrives at your location within 8 AM–11 PM, collects 2–3 mL of whole blood in an EDTA tube or one drop on an FTA card, and transports it in a temperature‑controlled cold chain immediately.
يتم سحب عينة دم وريدي عبر فني مختص معتمد في منزلك خلال ساعات العمل المحددة، وتُنقل تحت سلسلة تبريد آمنة حفاظاً على جودة الحمض النووي.
Pre‑ Preparation & Genetic Counselling
A genetic counselling session is mandatory before sample collection to draw a detailed pedigree chart of family members affected with AICA-ribosiduria due to ATIC deficiency. Provide a complete clinical history, including previous biochemical testing, imaging, and any medication list. No special fasting is required. If using an FTA card, ensure the blood drop is fully dried before packing. For patients with recent transfusion, notify our team to optimize sampling timing.
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