Test Price
900 AEDโ Home Collection Available
Hepatitis G Virus (HGV) RNA Detection PCR Test
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (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 Consultation for result interpretation with DHA-licensed specialists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Hepatitis G Virus (HGV) RNA Detection PCR Test utilizes real-time polymerase chain reaction (qPCR) to directly detect viral nucleic acid in plasma. This molecular assay is essential for confirming active viremia, monitoring co-infections, and guiding hepatology management for patients presenting with unexplained liver enzyme elevations.
| Parameter | HGV RNA PCR Test (DNA Labs UAE) | Standard HGV Antibody Test |
|---|---|---|
| Methodology | Real-Time PCR (qPCR) โ Nucleic Acid Amplification | ELISA / Rapid Immunoassay |
| Diagnostic Sensitivity | >99% (detects active viremia early) | ~85% (relies on antibody seroconversion) |
| Window Period | 2โ7 days post-exposure | 4โ12 weeks post-exposure |
| Turnaround Time | 18 days (comprehensive verification & ISO QC) | 1โ3 working days |
| Clinical Utility | Definitive diagnosis; guides antiviral & liver management | Screening only; cannot distinguish past from current infection |
Physician Insight & Safety Protocols
โAccurate molecular detection of HGV RNA is critical for differentiating active infection from past serological exposure. While this qPCR assay provides exceptional analytical sensitivity, results must be meticulously correlated with the patientโs full hepatic panel and clinical history to ensure precise therapeutic decision-making.โ
โ Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA ID: 9294403)
Advisory & Pre-Test Considerations
โ Do not discontinue any prescribed medication without consulting your doctor. This test does not replace specialist clinical evaluation.
Exclusion Criteria & Safety Checks
- Severe coagulopathy (INR >2.0) or platelet count <30,000/ยตL โ physician clearance required before venipuncture.
- Active chemotherapy or blood transfusion within 72 hours โ may interfere with test accuracy.
- Known bleeding disorders (e.g., hemophilia).
๐จ Emergency Red Flags โ Seek Immediate Medical Attention
- Sudden onset of deep jaundice, confusion, or abdominal swelling.
- Vomiting blood or coffee-ground material.
- Uncontrolled bruising or bleeding.
Patient FAQ & Clinical Guidance
1. What is the turnaround time for the HGV RNA PCR test?
The HGV RNA PCR test report is typically available within 18 days after sample collection, ensuring comprehensive verification and ISO quality control throughout the analytical process.
2. Do I need to fast before this test?
To ensure optimal plasma separation and reliable HGV RNA amplification, a 12-hour fasting period is recommended prior to your scheduled sample collection.
3. Can this test detect HGV infection in its early stages?
Yes, PCR detects HGV RNA within days of exposure, offering a definitive early diagnosis before antibodies become detectable. This narrow window period is critical for timely clinical intervention and management.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE strictly complies with the UAEโs legislative framework for health data and medical testing:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL).
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
- Federal Decree-Law No. 4 of 2016 on Medical Liability.
- ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
- All home collection services are performed by DHA-registered healthcare professionals under strict chain of custody protocols.
Clinical & Logistical Metadata
| Test Name | Hepatitis G Virus (HGV) RNA Detection PCR Test |
| Price (AED) | 900 AED |
| Turnaround Time | 18 Days |
| Sample Type / Matrix | Plasma (Peripheral Whole Blood) |
| Methodology Used | Real-Time PCR (qPCR) โ Nucleic Acid Amplification |
| ICD-10-CM Code | B19.9 |
| LOINC Code | 50683-9 |
| DHA Facility License & Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians