Test Price
800 AED✅ Home Collection Available
TORCH Panel Real-Time PCR in UAE | 800 AED | DHA Licensed
Executive Summary & Core Metrics
Accuracy Guarantee
99.9% Diagnostic Sensitivity via ISO Accredited Cold-Chain Processing
Premium Logistics
Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
Clinical Guidance
Telephonic Post-Test Clinical Guidance for Result Interpretation
Insurance Verification
Direct Billing Verification via WhatsApp +971 54 548 8731
Test Overview & Methodology
This advanced molecular panel detects congenital pathogens—Toxoplasma gondii, Rubella virus, Cytomegalovirus, and Herpes simplex virus types 1 and 2—using highly sensitive Real-Time PCR (qPCR) and End-Point PCR, ideal for prenatal screening and neonatal diagnosis. The test is performed on amniotic fluid or cord blood collected under sterile ultrasound guidance by a qualified clinician. A valid doctor’s prescription is required for non-surgical, non-pregnancy cases; fasting is not required.
| Feature | Our Test (Real-Time PCR) | Standard Serology (Alternative) |
|---|---|---|
| Method | Real-Time PCR (qPCR) + End-Point PCR + WGS confirmation | IgM/IgG antibody detection (ELISA) |
| Diagnostic Sensitivity | 99.9% – detects active infection DNA/RNA directly | Limited in early infection; false negatives possible |
| Turnaround Time | 1 week (Molecular Lab) | Often 2 weeks+ requiring confirmatory tests |
| Specialist Interpretation | Directly correlates with fetal health and treatment planning | Requires additional titre monitoring, ambiguity in acute vs. past infection |
Physician Insight & Safety Protocols
“As a clinician focusing on prenatal and infectious disease screening, I recommend the TORCH Panel Real-Time PCR for its superior sensitivity in detecting congenital infections directly from amniotic fluid or cord blood. Results must always be interpreted alongside maternal history, ultrasound markers, and clinical symptoms to guide timely intervention.”
— Dr. Ajay Singh, General Practitioner | DHA License ID: 36234132
Advisory & Safety Considerations
⚠️ Safety Notice & Exclusion Criteria
- Exclusion: Active bleeding disorders, uncontrolled hypertension, or critical illness require physician clearance before amniocentesis or cordocentesis.
- Emergency Red Flags: If you experience severe abdominal pain, fever above 38.5°C, vaginal bleeding, or fluid leakage after sample collection, seek immediate emergency care.
- Test must be performed and interpreted by a DHA-licensed laboratory; self-collection is not permitted.
Medication Advisory
Do not discontinue or alter any prescribed medication without prior consultation with your treating physician. Test results are for diagnostic guidance and do not replace professional medical advice.
Patient FAQ & Clinical Guidance
1. What infections does the TORCH Panel Real-Time PCR detect?
Our TORCH Panel Real-Time PCR simultaneously detects Toxoplasma gondii, Rubella virus, Cytomegalovirus, Herpes simplex virus types 1 and 2, and other congenital pathogens with 99.9% sensitivity. This molecular approach directly identifies pathogen DNA or RNA, eliminating the ambiguity of serological antibody tests.
2. How is the sample collected and is the procedure safe during pregnancy?
Amniotic fluid or cord blood is collected via sterile amniocentesis or cordocentesis under continuous ultrasound guidance by a qualified specialist, ensuring maternal-fetal safety. The procedure is performed exclusively within an accredited hospital setting.
3. Why choose your laboratory for TORCH PCR testing in the UAE?
We provide ISO-certified, DHA-accredited molecular testing with rapid 1-week turnaround time, hospital-based sterile collection, and telephonic post-test clinical guidance for result interpretation. Our dedicated team supports direct billing verification through WhatsApp.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates in full compliance with 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, ensuring that all patient data, test results, and clinical communications remain encrypted and confidential. Clinical safety and patient consent protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. All diagnostic procedures are performed under the regulatory oversight of the Dubai Health Authority (DHA) License No. 1143.
Clinical & Logistical Metadata
| Test Name | TORCH Panel Real-Time PCR |
| Price (AED) | 800 AED |
| Turnaround Time | 1 Week (Molecular Lab) |
| Sample Type / Matrix | Amniotic Fluid (via Amniocentesis) or Cord Blood (via Cordocentesis) – Hospital Extraction Only |
| Methodology Used | Real-Time PCR (qPCR), End-Point PCR, with reflex to Whole Genome Sequencing (WGS) confirmation |
| ICD-10-CM Code | Z13.83, O98.5 |
| LOINC Code | 78955-6 |
| 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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