Test Price
1,800 AED✅ Home Collection Available
Ribosomal P Antibody Test in UAE – 1800 AED
Executive Summary & Core Metrics
High-Definition Diagnostic Assurance
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO-certified processing and chemiluminescence immunoassay (CLIA).
- 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 clinical correlation with a DHA‑licensed general practitioner.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731 (DHA Facility License: 1143).
Test Overview & Methodology
Ribosomal P Antibody Test is a specialised autoimmune assay that detects autoantibodies against ribosomal P proteins, aiding in the diagnosis of neuropsychiatric systemic lupus erythematosus (NPSLE). In the UAE, this test is performed using state‑of‑the‑art chemiluminescence immunoassay (CLIA) under strict DHA/MOHAP accreditation.
| Feature | Our Test (Ribosomal P CLIA) | Conventional ELISA Alternative |
|---|---|---|
| Methodology | Chemiluminescence Immunoassay (High Sensitivity) | Enzyme‑Linked Immunosorbent Assay (Moderate Sensitivity) |
| Sample Requirement | 2 mL serum, cold‑chain shipped | 1‑2 mL serum, refrigerated only |
| Turnaround Time | 2‑3 weeks | 3‑4 weeks |
| Regulatory Status | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) & DHA Compliant | Basic lab certification |
Physician Insight & Safety Protocols
“As a DHA-licensed general practitioner, I remind patients that a positive Ribosomal P antibody test strongly correlates with neuropsychiatric lupus; however, results must always be interpreted alongside clinical history and other autoantibody profiles. Please never self‑diagnose based solely on this marker – a comprehensive rheumatology consultation is essential for personalised care.”
— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
Advisory – Medication Precautions
Do not discontinue prescribed medication without consulting your doctor. Abruptly stopping immunosuppressants or corticosteroids can trigger severe disease flares.
Exclusion Criteria & ER Red Flags
- Exclusion Criteria: Patients with unstable vital signs, severe coagulopathy, acute febrile illness, or inability to provide informed consent (including minors without legal guardian consent under UAE law).
- ER Red Flags – seek immediate emergency care if you experience: Acute confusion, hallucinations, suicidal ideation, seizures, or sudden severe headache with neurological deficits.
Patient FAQ & Clinical Guidance
1. What is the Ribosomal P antibody test used for?
Snippet: This test measures anti‑ribosomal P antibodies, highly specific biomarkers for lupus psychosis and cognitive dysfunction.
It is primarily employed in the evaluation of systemic lupus erythematosus (SLE), particularly when neuropsychiatric symptoms such as psychosis, mood disorders, or cognitive decline are present. The test aids rheumatologists in differentiating NPSLE from other causes of neurological disturbances, guiding timely immunomodulatory therapy.
2. How should I prepare for the Ribosomal P antibody test?
Snippet: No fasting required; a mandatory test send‑out consent form must be completed before blood collection.
The test requires a 2 mL serum sample collected in a serum separator tube (SST). It must be shipped refrigerated or frozen to the reference laboratory. A duly filled Test Send Out Consent Form (Form 35) is mandatory – our phlebotomist will provide this during home collection. Continue all regular medications unless explicitly advised otherwise by your physician.
3. What does a positive Ribosomal P antibody result mean?
Snippet: A positive result indicates high likelihood of neuropsychiatric lupus, especially psychosis, seizures, or cognitive dysfunction.
However, a positive test alone is not diagnostic; it must be correlated with anti‑dsDNA, ANA, and clinical criteria. Up to 50% of SLE patients with these antibodies may develop psychiatric manifestations. False positives are rare but can occur in other autoimmune conditions. Your rheumatologist will interpret the titre level in conjunction with your full clinical picture.
UAE Regulatory & Data Privacy Adherence
This test is performed in strict 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. Clinical safety and informed consent processes adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. All data is processed by DHA-licensed facilities (License: 1143) under ISO 9001:2015 certification. For home collection orders, a legal guardian must be present for patients under 18. Contact WhatsApp +971 54 548 8731 for insurance verification and booking.
Clinical & Logistical Metadata
| Test Name | Ribosomal P Antibody Test (CLIA) |
| Price (AED) | 1800 |
| Turnaround Time | 2–3 weeks |
| Sample Type / Matrix | Serum (2 mL SST) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection |
| Methodology Used | Chemiluminescence Immunoassay (CLIA) |
| ICD-10-CM Code | M32.9 (Systemic lupus erythematosus, unspecified), Z01.89 |
| LOINC Code | 13983-9 |
| DHA Facility License & Laboratory Address | Facility License: 1143 Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE Corporate Lab Branding: DNA Labs UAE |
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