Test Price
600 AED✅ Home Collection Available
TORCH Panel IgM Extended Test in UAE | 600 AED | DHA Licensed
Executive Summary & Core Metrics
- Accuracy Assurance: 99.9% diagnostic sensitivity via ISO‑certified dual‑platform processing (CLIA & EIA).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection available daily 8 AM – 11 PM.
- Clinical Guidance: Post‑test tele‑consultation with a DHA‑licensed General Practitioner to interpret results.
- Insurance: Direct insurance verification via WhatsApp at +971 54 548 8731.
- Turnaround Time: Same‑day result if serum collected Tuesday or Friday before 9 AM; otherwise 24–48 hours.
Test Overview & Methodology
The TORCH Panel IgM Extended Test is a comprehensive serologic screening for acute Toxoplasma, Rubella, Cytomegalovirus, and Herpes simplex infections. It is essential for evaluating recurrent pregnancy loss and congenital infection risk. The extended panel measures IgM antibodies via a combined CLIA and EIA dual‑platform approach, delivering high sensitivity and specificity in a single serum draw.
| Feature | Our Extended Panel | Standard Single Tests |
|---|---|---|
| Methodology | CLIA & EIA (dual‑platform, validated sensitivity) | EIA only; may miss borderline titres |
| Turnaround Time | Same day (if sample collected Tue/Fri by 9 AM) | 2–3 working days |
| Interpretive Support | Post‑test tele‑guidance by DHA‑licensed General Practitioner | Report only; no clinical correlation |
Physician Insight & Safety Protocols
Dr. Ajay Singh (DHA License: 36234132), General Practitioner, shares: "The TORCH IgM Extended Panel is a sensitive early marker, but positive IgM must always be correlated with IgG avidity, clinical presentation, and obstetric history. A single positive result does not confirm acute infection; close collaboration with your gynecologist is essential to avoid unnecessary interventions. Our home collection and tele‑guidance service ensures you receive timely, expert interpretation."
Advisory: Medication & Test Interference
Do not discontinue any prescribed medication without consulting your doctor. Immunosuppressive therapies (corticosteroids, biologics) and recent immunoglobulin infusions may produce false‑negative IgM results. Always disclose your full medication list to the collection team.
Exclusion Criteria & Safety Red Flags
- Postpone testing if you currently have a high fever or active febrile illness.
- Recent vaccination (especially rubella) can transiently elevate IgM – inform our clinical team before the draw.
- Emergency red flags: Seek immediate medical attention if you experience severe headache, vision loss, confusion, seizures, or difficulty breathing after sample collection, as these may indicate an acute infection requiring urgent care.
Patient FAQ & Clinical Guidance
1. What is the TORCH Panel IgM Extended Test used for?
This test detects acute IgM antibodies against Toxoplasma, Rubella, CMV, and HSV to evaluate recent or active infections that could cause congenital abnormalities or recurrent pregnancy loss. It is ordered primarily for women with a history of miscarriage or at risk of vertical transmission. The extended panel includes all four pathogens in a single serum draw, providing broader insight than individual assays.
2. How do I prepare for the test?
No fasting or special preparation is required; however, you must disclose all medications and supplements to ensure accurate interpretation. Certain drugs like immunosuppressants or recent immunoglobulin therapy may interfere with IgM detection. Our home collection team will review your history before the draw.
3. When will I receive my results?
If your serum sample is collected on Tuesday or Friday before 9 AM, the report is delivered the same day via our secure patient portal. Reports are accompanied by a DHA‑licensed tele‑guidance session to explain the clinical implications. Samples received after the cutoff are processed in the next batch and results are available within 24–48 hours.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance: DNA Labs UAE operates under DHA Facility License Number 1143 and adheres to Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) for all patient information. All health data handling complies with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical safety and patient consent follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Laboratory Address: Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE.
Clinical & Logistical Metadata
| Test Name | TORCH Panel IgM Extended Test |
| Price (AED) | 600 |
| Turnaround Time | Same day (Tue/Fri before 9 AM) or 24–48 hours |
| Sample Type / Matrix | Serum |
| Methodology Used | CLIA & EIA |
| ICD-10-CM Code | Z11.5 |
| LOINC Code | 24332-9 |
| DHA Facility License & Laboratory Address | License 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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