Test Price
100 AED✅ Home Collection Available
Phospholipid Antibody IgG Test in UAE | 100 AED | DHA-Licensed Diagnostic Laboratory
Executive Summary & Core Metrics
✓ 99.9% Diagnostic Sensitivity – ISO 9001:2015 accredited processing, fully compliant 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.
✓ Premium Home Collection – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM. ISO‑certified cold‑chain transportation ensures specimen integrity.
✓ Telephonic Clinical Guidance – Post‑test result interpretation by a DHA‑licensed General Practitioner.
✓ Insurance Verification – Submit your policy via WhatsApp to +971 54 548 8731 for direct billing confirmation.
Test Overview & Methodology
The Phospholipid Antibody IgG test is a high‑sensitivity quantitative enzyme immunoassay (ELISA) that detects IgG autoantibodies against phospholipids, which are implicated in antiphospholipid syndrome, thromboembolic disorders, and recurrent pregnancy loss. At our DHA‑licensed facility in Dubai Healthcare City, patients receive same‑day results supported by ISO 9001:2015 quality management systems and dedicated pre‑test tele‑guidance.
| Feature | Our Test (Phospholipid Antibody IgG ELISA) | Closest Alternative (Multi‑Panel Send‑out) |
|---|---|---|
| Precision / Methodology | Quantitative ELISA with internal DHA‑calibrated controls; 99.9% sensitivity | Qualitative/semi‑quantitative immunoblot; lower reproducibility |
| Turnaround Time | Same day (sample received by 9 AM, report by evening) | 3–5 working days due to external referral |
| Patient Convenience | Hospital‑grade home collection 8 AM–11 PM, cold‑chain transport, WhatsApp support | Clinic visit only; limited after‑hours availability |
Physician Insight & Safety Protocols
“As a DHA‑licensed General Practitioner, I emphasize that no single laboratory result replaces a thorough clinical evaluation. Positive phospholipid antibody findings must be correlated with your complete medical history, presenting symptoms, and additional coagulation profile studies. Our team is committed to guiding you with empathy and evidence‑based precision throughout the diagnostic pathway.”
— Dr. Ajay Singh | General Practitioner | DHA Registration ID: 36234132
⚠️ Important Advisory – Medication Continuity
Do not discontinue any prescribed anticoagulant or antiplatelet medication without explicit instruction from your treating physician. This diagnostic test does not replace clinical management of thrombotic disorders.
Exclusion Criteria & Emergency Red Flags
- Home collection is not suitable if you are experiencing acute chest pain, shortness of breath, leg swelling with redness, or sudden neurological symptoms — call 998 or proceed to the nearest Emergency Department immediately.
- Notify our team before booking if you have severe anemia, active bleeding, or uncontrolled hypertension; a hospital‑based draw may be advised as a precaution.
- Minors require guardian consent in compliance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Patient FAQ & Clinical Guidance
1. What is the Phospholipid Antibody IgG test used for?
This test detects IgG phospholipid antibodies to help confirm antiphospholipid syndrome in patients with clotting disorders. It aids in evaluating unexplained venous or arterial thrombosis and recurrent miscarriages, enabling timely intervention by gynecologists, cardiologists, and rheumatologists.
2. How should I prepare for the test?
No special preparation is required; however, please disclose any blood thinners or anticoagulant medications to your physician prior to testing. Routine sample collection uses a standard SST tube; you may continue your usual diet and medications unless otherwise directed by your doctor.
3. What do positive results mean?
Positive IgG antibodies suggest antiphospholipid syndrome and typically warrant confirmatory testing along with a specialist clinical assessment. A positive finding is not a stand‑alone diagnosis; repeat testing after 12 weeks and correlation with clinical criteria are essential. Your reporting physician will provide telephonic guidance on the appropriate next steps.
UAE Regulatory & Data Privacy Adherence
Data Protection & Health Information Governance
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. All patient data, including test results and personal identifiers, are encrypted, access‑controlled, and processed exclusively within the UAE jurisdiction. No information is shared with third parties without explicit patient consent as required by law.
Our DHA‑licensed facility (License No. 1143) adheres to ISO 9001:2015 quality management standards and undergoes regular audits to ensure continuous compliance with all applicable federal and local healthcare regulations.
Clinical & Logistical Metadata
| Test Name | Phospholipid Antibody IgG |
| Price (AED) | 100 |
| Turnaround Time | Same Day (sample received by 9 AM; report delivered by evening) |
| Sample Type / Matrix | Serum (Standard Venipuncture) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM |
| Methodology Used | Quantitative Enzyme Immunoassay (ELISA) |
| ICD-10-CM Code | D68.61 |
| LOINC Code | 17706-4 |
| DHA Facility License & Laboratory Address | DHA Facility License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians