Test Price
1,500 AED✅ Home Collection Available
TORCH DNA Detection Test (PCR) in UAE | 1500 AED | DHA-Approved
Executive Summary & Core Metrics
- Accuracy: 99.9% diagnostic sensitivity and specificity via ISO 15189-accredited real-time PCR methodology.
- Logistics: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility (e.g., amniocentesis, lumbar puncture for CSF); mobile home phlebotomy is disabled for safety.
- Clinical Guidance: Free telephonic post-test interpretation with a DHA-licensed General Practitioner.
- Insurance: Pre-verification of direct billing via WhatsApp +971 54 548 8731 before scheduling.
Test Overview & Methodology
The TORCH DNA Detection Test employs quantitative real-time PCR (qPCR) with melt-curve analysis to qualitatively detect nucleic acids of Toxoplasma gondii, Rubella virus, Cytomegalovirus, and Herpes simplex virus types 1/2 in amniotic fluid or cerebrospinal fluid (CSF). This molecular approach directly identifies pathogen genome, bypassing the serological window period and cross-reactivity limitations common to IgM/IgG assays. The result is reported as presence or absence of each target with cycle threshold (Ct) values, supporting confirmatory diagnosis of congenital and perinatal infections.
Comparative Diagnostic Methods
| Feature | TORCH DNA (qPCR) – Our Test | Standard Serology (IgM/IgG ELISA) |
|---|---|---|
| Analytical Specificity | 99.9% – direct pathogen genome detection | Variable; false positives from cross-reactive antibodies |
| Window Period Sensitivity | Detectable immediately after infection (acute phase) | Seroconversion lag of 2–4 weeks |
| Turnaround Time | 8 days from sample receipt (morning cutoff 11 AM) | 2–5 days; frequent indeterminate results require repeat testing |
Physician Insight & Safety Protocols
From Dr. Ajay Singh (DHA License: 36234132) – “A positive TORCH PCR result must be correlated with maternal history, gestational age, and fetal imaging. This test detects the presence of pathogen DNA, not severity of infection or fetal prognosis. Always discuss the result with your obstetrician before any therapeutic or interventional decisions.”
Clinical Advisory: Hospital-Only Collection
Exclusion Criteria & Safety Red Flags
- Amniocentesis is contraindicated in the presence of ruptured membranes, active cervical incompetence, or chorioamnionitis.
- CSF collection (lumbar puncture) should be avoided in patients with thrombocytopenia, coagulopathy, or signs of elevated intracranial pressure (e.g., papilledema).
- Seek immediate emergency care if you experience severe abdominal pain, high fever, fluid leakage, or preterm labour contractions after an invasive procedure.
Patient FAQ & Clinical Guidance
1. What does the TORCH DNA test detect?
It qualitatively detects the DNA of Toxoplasma, Rubella, CMV, and HSV-1/2 in amniotic fluid or CSF using real-time PCR technology. The report shows a positive or negative result for each pathogen, along with Ct values for clinical correlation.
2. Why is PCR preferred over serology for congenital TORCH infections?
PCR directly identifies the pathogen genome, eliminating the serological window period and cross-reactivity with other antibodies. It provides a definitive molecular diagnosis essential for guiding antenatal management.
3. Do I need to fast or prepare before sample collection?
No fasting is required. However, because the sample is obtained via amniocentesis or lumbar puncture, you must be at a licensed hospital. Do not freeze the sample; it must be kept cool (2–8°C) and delivered immediately to the laboratory.
4. How much does the test cost and how do I pay?
The test costs 1,500 AED. We verify direct billing with your insurance provider before scheduling. For cash payments or insurance queries, contact our billing team via WhatsApp at +971 54 548 8731.
5. How long does it take to get results and who can interpret them?
Results are available within 8 days from sample receipt. Our DHA-licensed General Practitioner provides free telephonic post-test guidance to help you understand the clinical implications of the report.
UAE Regulatory & Data Privacy Adherence
Legal & Compliance Framework
All patient data and clinical processes 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. Diagnostic procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. The laboratory is fully licensed by the Dubai Health Authority (DHA) under facility number 1143.
Clinical & Logistical Metadata
| Test Name | TORCH DNA Detection Test (Real-Time PCR) |
| Price (AED) | 1,500 |
| Turnaround Time | 8 days |
| Sample Type / Matrix | Amniotic fluid or cerebrospinal fluid (CSF) |
| Methodology Used | Quantitative Real-Time PCR (qPCR) with melt-curve analysis |
| ICD-10-CM Code | O98.5 (Other viral diseases complicating pregnancy) |
| LOINC Code | 74818-3 (TORCH panel – Amniotic fluid) |
| DHA Facility License & Lab Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians