Test Price
2,800 AEDโ Home Collection Available
RUNX1 Gene Platelet Disorder with Associated Myeloid Malignancy Genetic Test in UAE
Executive Summary & Core Metrics
๐ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
๐ Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
๐ฉบ Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
๐ณ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This advanced genetic test analyzes the RUNX1 gene to detect germline mutations linked to familial platelet disorder with predisposition to acute myeloid leukemia (AML). It provides a comprehensive risk assessment and personalized clinical management for hematologic malignancy surveillance.
| Feature | Our Test (NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | 99.9% Diagnostic Sensitivity | ~95% for targeted regions |
| Method | NGS (full gene coverage, incl. non-coding regions) | Sanger sequencing, hotspot analysis only |
| Turnaround | 3 โ 4 Weeks | 4 โ 6 Weeks |
Physician Insight & Safety Protocols
"Molecular confirmation of a RUNX1 germline mutation fundamentally transforms the clinical surveillance framework for the patient and their at-risk family members. A multidisciplinary approach involving genetic counseling, serial hematological assessments, and long-term monitoring is paramount to optimizing outcomes."
โ Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
โ ๏ธ Medication Safety Advisory
Do not discontinue prescribed medication without consulting your doctor.
๐ Safety Exclusion & ER Red Flags
- Exclusion Criteria: Active bleeding, acute infection, recent blood transfusion, or ongoing chemotherapy that may affect DNA quality.
- ER Red Flags: Sudden severe bleeding, newโonset petechiae, unexplained bruising, neurological symptoms (severe headache, vision changes), or fever with bleeding/bruising.
Patient FAQ & Clinical Guidance
1. What is the purpose of the RUNX1 Genetic Test?
This test identifies inherited RUNX1 mutations to assess risk for platelet disorder and myeloid malignancy. It enables early intervention, tailored surveillance, and informed family planning.
2. How is the sample collected and what is the turnaround time?
Peripheral whole blood or FTA card collection through our VIP Mobile Phlebotomy service ensures sample integrity via temperature-controlled cold-chain logistics. Results are reliably delivered within 3 to 4 weeks.
3. Are genetic counseling and insurance coverage available?
Pre- and post-test genetic counseling is integral to the service, thoroughly interpreting family history and implications. Insurance billing is verified directly via WhatsApp, with direct billing coordination for major UAE insurers.
UAE Regulatory & Data Privacy Adherence
Data security and patient privacy are governed by Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical safety and patient consent protocols strictly adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. DNA Labs UAE operates under DHA Facility License Number 1143.
Clinical & Logistical Metadata
| Test Name | RUNX1 Gene Platelet Disorder with Associated Myeloid Malignancy Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 โ 4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood or FTA Card |
| Methodology Used | Next-Generation Sequencing (NGS) โ Full Gene Coverage |
| ICD-10-CM Code | Z15.09 |
| LOINC Code | 82993-7 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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HIPAA
All reports reviewed by DHA-Certified physicians