Test Price
4,800 AED✅ Home Collection Available
WS1 Full Gene Sequence Analysis (Wolfram Syndrome, DIDMOAD) in UAE | 4800 AED | 2026 DHA Guidelines
تحليل التسلسل الجيني الكامل لجين WS1 (متلازمة ولفرام - ديدمواد) في الإمارات | 4800 درهم | معتمد من هيئة الصحة بدبي
ملخص تنفيذي: ضمان الدقة 99.9% من خلال معالجة معتمدة ISO، خدمة منزلية فاخرة، وإرشاد طبي بعد الفحص.
- ✓ 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 and VIP Mobile Phlebotomy (8 AM – 11 PM).
- ✓ Clinical Guidance: Telephonic Post-Test Clinical Guidance by a DHA-licensed specialist interpreting your results.
- ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Overview
This advanced genetic test sequences the entire WFS1 gene to confirm or rule out Wolfram syndrome (DIDMOAD) – a rare autosomal recessive disorder characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. Our NGS-based analysis provides comprehensive variant detection across all exons and exon‑intron boundaries.
تحليل جيني متطور يفحص الجين الكامل WFS1 لتشخيص متلازمة ولفرام (ديدمواد) بدقة استثنائية.
| Feature | Our Test (AME) | Closest Alternative |
|---|---|---|
| Methodology | Next Generation Sequencing (NGS) | Sanger Sequencing (single exon) |
| Analytical Sensitivity | >99.9% for SNVs & small indels | ~95% in targeted regions |
| Turnaround Time | 4–6 weeks | 6–8 weeks (if full gene by Sanger) |
Physician Insight & Safety Protocol
“As a clinician, I emphasise that a positive result confirms the genetic predisposition, but clinical correlation with endocrinological, ophthalmological, and audiological assessments remains essential for a definitive diagnosis. Patients and families should be counselled about the autosomal recessive inheritance pattern and the variable expressivity of this syndrome.”
— Dr. PRABHAKAR REDDY (DHA License: 61713011)
Medication Warning
Do not discontinue prescribed medication without consulting your doctor.
Safety Exclusion Criteria & Emergency Red Flags
- This test is not intended for surgical clearance, travel fitness certification, or pregnancy risk assessment.
- Invasive sample collection (amniotic fluid/chorionic villi) must follow obstetric guidelines and is not performed without prior counselling.
- If you experience sudden severe vision loss, rapidly progressing hearing impairment, or refractory diabetic ketoacidosis, seek emergency care immediately – do not wait for test results.
- For minors, genetic testing requires informed parental consent in compliance with UAE CDS Law 2026.
Patient FAQ & Clinical Guidance
1. What is WS1 full gene sequence analysis and why is it ordered?
Core answer (15‑word snippet): It is a genetic test that reads the entire WFS1 gene to diagnose Wolfram syndrome (DIDMOAD).
Clinicians order this test when a patient presents with coexisting diabetes mellitus, optic atrophy, deafness, or a positive family history to confirm the diagnosis at a molecular level and guide multidisciplinary management.
اختبار جيني يفحص كامل جين WFS1 لتأكيد تشخيص متلازمة ولفرام (ديدمواد) لدى المرضى الذين يعانون من السكري وضمور البصر وفقدان السمع.
2. What sample types are accepted, and how is the collection performed at home?
Core answer (15‑word snippet): We accept peripheral blood, amniotic fluid, chorionic villi, or cord blood for this analysis.
For home collection, a DHA-licensed phlebotomist arrives within a 8 AM–11 PM slot, properly identifies the patient, draws the required sample under strict aseptic conditions, and transports it in a temperature‑controlled cool box. Pre‑ counselling is conducted telephonically before the appointment.
نقبل عينات الدم المحيطي، السائل الأمنيوسي، الزغابات المشيمية، أو دم الحبل السري. يتم جمعها منزلياً بواسطة فني معتمد تحت شروط تعقيم صارمة.
3. How long do results take, and how will I receive my report?
Core answer (15‑word snippet): Results are delivered in 4–6 weeks via secure online portal and a teleconsultation call.
The diagnostic report includes variant description, zygosity, ACMG classification, and a clinical interpretation. You will receive an email alert once the report is ready; a DHA‑licensed genetic counsellor then calls you to explain findings, answer questions, and coordinate follow‑up with your referring physician.
تصدر النتائج خلال ٤–٦ أسابيع عبر بوابة إلكترونية آمنة مع استشارة هاتفية من أخصائي وراثة معتمد من هيئة الصحة بدبي.
This service complies with Federal Decree‑Law No. 41 of 2024 (Art. 87) on genetic data protection, UAE Personal Data Protection Law (PDPL), and CDS Law 2026 concerning minors' genetic testing.
Facility License: 9834453 | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | 2026 ICD‑10‑CM: Q87.8, Z15.0, Z13.7 | LOINC: 95419-5
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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.
Available in Arabic, English, Hindi & Urdu
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All reports reviewed by DHA-Certified physicians