Test Price
2,800 AED✅ Home Collection Available
WAS Gene (X‑Linked Intermittent Thrombocytopenia) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين WAS (قلة الصفيحات المرتبطة بالكروموسوم X المتقطعة) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity – NGS performed in ISO 9001:2015 certified lab.
- Premium Logistics: Hospital-Grade Home Collection (8 AM–11 PM) via ISO Cold-Chain & VIP Mobile Phlebotomy.
- Clinical Guidance: Complimentary telephonic post‑test result interpretation with a genetic counsellor.
- Insurance: Direct Billing Verification – WhatsApp +971 54 548 8731.
الملخص التنفيذي
يُجرى التحليل الجيني لجين WAS بتقنية التسلسل الجيني المتطورة (NGS) بدقة تشخيصية تبلغ 99.9% في مختبر معتمد من هيئة الصحة بدبي وموثق بشهادة ISO 9001:2015. يتضمن خدمة سحب منزلي فاخرة وفق سلسلة تبريد معتمدة، ودعم استشاري جيني هاتفي بعد النتيجة، وتدقيق تغطية التأمين الصحي عبر الواتساب.
Clinical Overview & Test Comparison
This advanced Next‑Generation Sequencing (NGS) test analyses the entire WAS gene for pathogenic variants linked to X‑linked intermittent thrombocytopenia (XLT) – a hereditary bleeding disorder characterised by low platelet counts with normal platelet size. It confirms diagnosis, guides personalised management, and enables accurate carrier testing and genetic counselling for family members.
يُحلل اختبار تسلسل الجين الكامل طفرات جين WAS المسببة لقلة الصفيحات الوراثية المرتبطة بالكروموسوم X، ويساعد في تأكيد التشخيص وتخطيط الإجراءات العلاجية والفحوصات الأسرية.
| Feature | Our NGS Test (Enhanced) | Closest Alternative |
|---|---|---|
| Methodology | Whole‑Gene NGS with Copy Number Variation (CNV) calling; 2026 standard LC‑MS/MS‑grade library prep | Sanger sequencing (targeted exons only) – limited to single nucleotide variants |
| Analytical Sensitivity | 99.9% for SNVs, indels & exonic deletions/duplications | ~95% for point mutations; misses large rearrangements |
| Turnaround Time | 3–4 Weeks (cold‑chain home collection included) | 4–6 Weeks (hospital visit required) |
| DHA/MOHAP Accreditation | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) & DHA CLIA equivalent | May lack UAE‑specific quality certification |
Physician Insight & Safety Protocol
“As a practising hematologist, I understand the anxiety that an inherited bleeding disorder can bring. This NGS test provides definitive molecular answers, but all results must be interpreted in the context of your full clinical picture and family history. Never stop any prescribed medication without first discussing it with your doctor.”
— Dr. PRABHAKAR REDDY, DHA License 61713011
Medication Warning
Do not discontinue prescribed medication without consulting your physician. This test does not replace routine clinical follow‑up or emergency care.
Exclusion Criteria & Emergency Red Flags
Exclusion Criteria (Do NOT proceed without clearance):
- Inability to provide informed consent (minors require legal guardian as per UAE CDS Law 2026).
- Allogeneic blood transfusion within the last 2 weeks (may confound DNA analysis if whole blood used).
- Known active infection or acute haemolysis requiring immediate treatment.
Seek Emergency Care Immediately If:
- Uncontrolled bleeding, spontaneous bruising, or prolonged bleeding after minor trauma.
- Sudden severe headache, confusion, or focal neurological signs (risk of intracranial haemorrhage).
- High fever with petechiae or purpura (possible secondary infection).
Frequently Asked Questions
1. What exactly is the WAS gene NGS test, and why is it necessary?
ما هو اختبار جين WAS ولماذا أحتاجه؟
Snippet: The WAS gene NGS test sequences the entire WAS gene to identify pathogenic mutations causing X‑linked intermittent thrombocytopenia, guiding precise diagnosis, treatment, and family risk assessment. Additional genetic counselling is recommended before and after testing to interpret the results fully.
2. How is the sample collected, and is home collection safe?
كيف تُجمع العينة وهل السحب المنزلي آمن؟
Snippet: A certified phlebotomist visits your home using an ISO cold‑chain kit to collect a small blood sample, extracted DNA, or a single blood drop on an FTA card, ensuring sample integrity and absolute safety. The entire process adheres to DHA infection control standards and is completed in under 15 minutes.
3. Will my insurance cover this genetic test, and what if I need help interpreting results?
هل يشمل التأمين هذا الاختبار وماذا عن تفسير النتائج؟
Snippet: Our team verifies insurance coverage directly via WhatsApp at +971 54 548 8731, and a post‑ telephonic session with a DHA‑licensed genetic counsellor is included to explain your results and next clinical steps. No patient is left without clear, actionable guidance.
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