Test Price
2,800 AED✅ Home Collection Available
ARX Gene Sequencing (Hydranencephaly with Abnormal Genitalia / X‑Linked Lissencephaly Type 2) Genetic Test in UAE | 2 800 AED | 2026 DHA Guidelines
تحليل تسلسل جين ARX لمرض انعدام الدماغ مع تشوهات تناسلية وانعدام التلافيف المرتبط بالكروموسوم X (النوع 2) بالإمارات | 2 800 درهم | معتمد من هيئة الصحة بدبي 2026
Executive Summary | ملخص تنفيذي
يُقدِّم مختبرنا المُعتمد دولياً اختبار تسلسل جين ARX بدقة تشخيصية تصل إلى 99.9% وفقاً لمعايير الآيزو 9001:2015. يشمل السعر خدمة السحب المنزلي بتقنية التبريد المعتمدة واستشارة وراثية هاتفية بعد النتيجة. Our ISO‑accredited molecular genetics facility delivers 99.9% diagnostic sensitivity for ARX gene mutations using next‑generation sequencing (NGS). The 2 800 AED package integrates hospital‑grade cold‑chain home collection, VIP phlebotomy, and post‑test clinical guidance.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑certified processing (EN/ISO 9001:2015).
- Premium Logistics: Paid Hospital‑Grade Home Collection with ISO‑certified cold‑chain and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic post‑test result interpretation and genetic counselling.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Overview
This advanced NGS test fully sequences the ARX (aristaless‑related homeobox) gene to detect pathogenic variants responsible for hydranencephaly with abnormal genitalia and X‑linked lissencephaly type 2. Combined with pre‑test genetic counselling, the analysis provides a definitive molecular diagnosis that guides neurodevelopmental prognosis, endocrine management, and family planning decisions. يُتيح هذا التحليل التسلسل الكامل لجين ARX لتشخيص الحالات النادرة بدقة عالية وتوجيه خطة الرعاية السريرية والاستشارات الوراثية للأسر المتضررة.
| Feature | Our ARX NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision / Method | Full‑gene NGS with deletion/duplication analysis | Single‑exon Sanger sequencing; limited CNV detection |
| Turnaround Time | 3 to 4 weeks | 4 to 6 weeks |
| Sample Requirements | Whole blood, extracted DNA, or one drop on FTA card | Whole blood or extracted DNA only |
| Cost | 2 800 AED | ~3 200 AED |
| Regulatory Compliance | Fully aligned with UAE Decree‑Law No. 41/2024, CDS Law 2026, PDPL | Varies by provider |
Physician Insight & Safety Protocol
“As a DHA‑licensed genetic medicine specialist, I stress that ARX gene results must be interpreted together with neuroimaging, full clinical examination, and endocrine work‑up. A positive finding can clarify the child’s neurodevelopmental trajectory and enable informed reproductive choices, but it should never be viewed in isolation. Clinical correlation remains paramount.”
— Dr. Prabhakar Reddy, DHA License: 61713011
Do not discontinue any prescribed antiepileptic drugs, steroids, or other medications without consulting the treating physician. Genetic results may influence therapeutic choices, but abrupt cessation can be life‑threatening.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Inability to obtain informed consent (for minors, mandatory legal guardian consent as per UAE CDS Law 2026). Severe thrombocytopenia or bleeding disorder that precludes safe phlebotomy.
- ER Red Flags: New‑onset prolonged seizures or status epilepticus; signs of acute adrenal insufficiency (vomiting, dehydration, shock) – especially if adrenal hypoplasia congenita is suspected; severe electrolyte imbalance with ambiguous genitalia.
Patient FAQ & Clinical Guidance
Q1: What does the ARX gene NGS test identify and how does it benefit my child?
Snippet Answer: This test sequences the entire ARX gene to detect variants causing hydranencephaly and lissencephaly, enabling precise diagnosis, prognosis, and reproductive planning.
س: ماذا يكشف اختبار جين ARX بالتسلسل الجيني وكيف يفيد طفلي؟
ج: يكشف الاختبار التسلسل الكامل لجين ARX لتحديد الطفرات المسبّبة لانعدام الدماغ وتشوهات الأعضاء التناسلية وانعدام التلافيف، مما يمكّن من التشخيص الدقيق وتوجيه الخطة العلاجية والاستشارات الوراثية.
Q2: How is the sample collected and what is the turnaround time?
Snippet Answer: A blood sample or a drop of blood on an FTA card is collected at home by a certified phlebotomist, and results are delivered in 3–4 weeks.
س: كيف تُجمَع العيّنة وما هو زمن النتيجة؟
ج: يتم سحب عيّنة دم أو قطرة دم على بطاقة FTA في المنزل بواسطة ممرّض معتمد، وتصدر النتيجة خلال ٣ إلى ٤ أسابيع.
Q3: Are test results covered by UAE health insurance for genetic disorders?
Snippet Answer: Many UAE insurance plans cover medically necessary genetic tests; we provide direct billing verification via WhatsApp to confirm your coverage.
س: هل يغطي التأمين الصحي في الإمارات هذا الاختبار الجيني؟
ج: تغطي العديد من خطط التأمين في الإمارات الاختبارات الجينية الضرورية طبياً؛ نقدم خدمة التحقق من التغطية المباشرة عبر الواتساب.
Pre‑ Requirements
Prior to sample collection, a genetic counselling session is mandatory to draw a detailed pedigree chart of family members affected by ARX‑related conditions. The clinical history of the patient must be provided. Samples accepted: whole blood, extracted DNA, or one drop of blood on FTA card.
This service strictly complies with Federal Decree‑Law No. 41 of 2024 (Art. 87) on genetic testing consent, UAE Child Data Safety (CDS) Law 2026 for minors, and the UAE Personal Data Protection Law (PDPL). Laboratory certified ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) and holding DHA facility license 9834453.
Clinical consultation line & WhatsApp: +971 54 548 8731. Home collection available 8 AM – 11 PM daily.
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.
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All reports reviewed by DHA-Certified physicians