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Test Price

1,200 AED

✅ Home Collection Available

Autoimmune Hepatitis Panel in UAE | 1,200 AED | DHA Licensed Laboratory

Executive Summary & Core Metrics

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139). Method: Indirect Immunofluorescence Assay (IFA) on triple tissue substrates.
  • Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (8 AM – 11 PM). Temperature-controlled transport from your doorstep to the lab.
  • Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance by a DHA-licensed physician to interpret your results in clinical context.
  • Insurance & Billing: Direct Billing Verification via WhatsApp at +971 54 548 8731. Pre-approval confirmation before sample collection.

Test Overview & Methodology

This panel uses Indirect Immunofluorescence Assay (IFA) to detect serum autoantibodies — anti-smooth muscle, anti-LKM-1, anti-LC-1, and ANA — characteristic of autoimmune hepatitis. It is the foundational serological step for differentiating autoimmune liver disease from viral or drug-induced hepatitis, with results available the next day after sample receipt.

ParameterOur Autoimmune Hepatitis PanelBasic Autoimmune Screen (Alternative)
PrecisionIFA on 3 substrates (Rodent Stomach/Kidney/Liver) — detects pattern-specific titersELISA-based single antigen screening — lower sensitivity for non-typical antibodies
MethodIndirect Immunofluorescence Assay (IFA) — gold standard protocolEnzyme Immunoassay (EIA) — may miss conformational epitopes
SpeedSample by 11 AM → Report next day48–72 hours typical
RegulatoryISO 9001:2015, Federal Decree-Law No. 45 of 2021 (PDPL), Federal Law No. 2 of 2019Often lacks local DHA accreditation

Physician Insight & Safety Protocols

“As a DHA-licensed general practitioner, I emphasize that this panel is an essential first step for evaluating suspected autoimmune liver disease. Results must be interpreted in conjunction with liver biochemistry, imaging, and occasionally liver biopsy. A negative IFA does not exclude autoimmune hepatitis if clinical suspicion remains high — always share your results with your specialist for a complete assessment.” — Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132

Medication Advisory

⚠️ Important Medication Notice

Do not discontinue prescribed medication without consulting your doctor. Immunosuppressants can alter antibody titers and may affect test interpretation. Always inform your phlebotomist about all current medications before sample collection.

Exclusion Criteria & Emergency Red Flags

  • Active febrile illness or acute hepatitis symptoms — immediate physician evaluation required before proceeding.
  • Severe coagulopathy or ongoing bleeding — venous sampling risk must be assessed by a clinician.
  • If you develop sudden jaundice, confusion, or severe abdominal pain, seek emergency care immediately; do not rely solely on this panel for acute management.

Patient FAQ & Clinical Guidance

1. What does the Autoimmune Hepatitis Panel detect and why is it ordered?

The panel detects circulating autoantibodies (anti-smooth muscle, anti-LKM-1, anti-LC-1, and ANA) using high-sensitivity IFA on triple tissue substrates. It is ordered to differentiate autoimmune hepatitis from viral, drug-induced, or metabolic liver disease when patients present with elevated liver enzymes and compatible clinical features.

2. Is fasting required before sample collection and how should I prepare?

No special preparation or fasting is needed. A 3 mL serum sample is drawn from an SST tube. You may eat and drink normally unless your physician advises otherwise for other concurrent tests.

3. How are results reported and what do they mean?

Results are reported as antibody titers with pattern descriptions (e.g., anti-smooth muscle positive at 1:80). Definitive diagnosis requires integration with liver enzymes (ALT, AST, ALP, GGT), total bilirubin, and expert clinical correlation by your gastroenterologist or hepatologist.

4. How long does it take to get results and how will I receive them?

Samples received by 11 AM are processed and reported by the next business day. Results are delivered via secure email and SMS notification. A complimentary telephonic consultation with a DHA-licensed physician is scheduled to help you understand your report.

UAE Regulatory & Data Privacy Adherence

DNA Labs UAE operates under DHA Facility License Number 1143 and adheres to the highest standards of data protection and healthcare compliance. All patient data is processed in full accordance 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 patient consent protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability. Your health information is encrypted, access-controlled, and never shared without your explicit consent.

Our laboratory is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139), ensuring rigorous quality management across all pre-analytical, analytical, and post-analytical processes.

Clinical & Logistical Metadata

Test Name Autoimmune Hepatitis Panel
Price (AED) 1,200 AED
Turnaround Time Next business day (sample by 11 AM)
Sample Type / Matrix Serum (SST tube, 3 mL)
Methodology Used Indirect Immunofluorescence Assay (IFA) on triple tissue substrates
ICD-10-CM Code K75.4 (Autoimmune hepatitis)
LOINC Code 100336-1 (Autoimmune hepatitis panel - Serum)
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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