Test Price
2,800 AED✅ Home Collection Available
WAS Gene (X‑Linked Intermittent Thrombocytopenia) Genetic Test in UAE | 2,800 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity – NGS performed in ISO 9001:2015 certified laboratory (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM.
- Clinical Guidance: Complimentary telephonic post-test result interpretation with a DHA-licensed genetic counsellor.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
- DHA License: Facility License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE.
Test Overview & Methodology
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. The assay confirms diagnosis, guides personalised management, and enables accurate carrier testing and genetic counselling for family members. Whole‑gene NGS with copy number variation (CNV) calling delivers comprehensive detection of single nucleotide variants, small insertions/deletions, and exonic rearrangements in a single workflow.
| Feature | Our NGS Test (Enhanced) | Closest Alternative |
|---|---|---|
| Methodology | Whole‑Gene NGS with CNV calling; high‑fidelity library preparation | 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 (home collection included) | 4–6 Weeks (hospital visit required) |
| DHA Accreditation | ISO 9001:2015 & DHA Facility License No. 1143 | May lack UAE‑specific quality certification |
Physician Insight & Safety Protocols
“Genetic testing for WAS gene variants offers definitive molecular diagnosis for X‑linked intermittent thrombocytopenia, enabling precise clinical management and informed family counselling. As a consultant in medical genetics, I emphasise that all genetic results must be interpreted within the broader clinical context and discussed with a qualified specialist before any treatment decisions are made.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics | DHA Registration ID: 9294403
Clinical Advisory – Medication & Follow‑Up
Medication & Clinical Follow‑Up Advisory
Do not discontinue any prescribed medication or alter your treatment regimen without consulting your physician. This genetic test does not replace routine clinical follow‑up or emergency care. Always maintain regular appointments with your haematologist or genetic specialist.
Exclusion Criteria & Emergency Red Flags
Exclusion Criteria (Do NOT proceed without clearance):
- Inability to provide informed consent (minors require a legal guardian).
- Allogeneic blood transfusion within the last 2 weeks (may confound DNA analysis if whole blood is 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).
Patient FAQ & Clinical Guidance
1. What is the WAS gene NGS test and why is it necessary?
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. Comprehensive genetic counselling is recommended before and after testing to interpret the results fully and plan appropriate clinical management.
2. How is the sample collected and is home collection safe?
A certified phlebotomist visits your home using a temperature‑controlled cold‑chain kit to collect a small blood sample, ensuring sample integrity and absolute safety. The entire process adheres to DHA infection control standards and is completed in under 15 minutes. VIP Mobile Phlebotomy is available daily from 8 AM to 11 PM.
3. Will my insurance cover this genetic test and how do I interpret the results?
Our team verifies insurance coverage directly via WhatsApp at +971 54 548 8731. A complimentary telephonic session with a DHA‑licensed genetic counsellor is included to explain your results and recommend next clinical steps. No patient is left without clear, actionable guidance.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates in full compliance with UAE federal data protection and healthcare information security laws:
- Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) – governing the collection, processing, and storage of personal health data.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – regulating health information systems and data confidentiality.
- Federal Decree‑Law No. 4 of 2016 on Medical Liability – establishing clinical testing safety standards and patient consent requirements.
All genetic data is encrypted, access‑controlled, and retained only for the lawful period required by UAE regulations.
Clinical & Logistical Metadata
| Test Name | WAS Gene (X‑Linked Intermittent Thrombocytopenia) NGS Analysis |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood – VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection (daily 8 AM – 11 PM) |
| Methodology Used | Next‑Generation Sequencing (NGS) with Copy Number Variation (CNV) calling |
| ICD-10-CM Code | D69.4 |
| LOINC Code | 103204-5 |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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