Autoimmune Encephalitis Panel CSF Test – Dubai, UAE | 3000 AED

Executive Summary & Core Metrics

✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing (Cell‑Based Assay with IFA).
✓ Collection Protocol: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
✓ Clinical Guidance: Telephonic Post‑Test Clinical Guidance in result interpretation by DHA‑licensed General Practitioner.
✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The Autoimmune Encephalitis Panel (CSF) detects pathogenic neural autoantibodies in cerebrospinal fluid using a cell‑based assay (CBA) with indirect immunofluorescence (IFA). This panel covers the most common antibodies associated with autoimmune encephalitis (e.g., anti‑NMDA, anti‑LGI1, anti‑CASPR2, anti‑GABAB), enabling precise diagnosis and targeted immunotherapy.

Feature	Our Panel (Premium CSF)	Standard Serum ELISA
Methodology	Cell‑Based Assay + IFA + confirmatory immunoblot	Indirect ELISA only
Diagnostic Sensitivity	99.9% (ISO validated)	~85%
Turnaround Time	Same day (if sample received Tue/Fri by 9 AM)	3–5 working days
Sample Handling	Refrigerated/frozen cold‑chain, GDP‑compliant	Ambient, risk of degradation
UAE Regulatory	DHA/MOHAP approved, ISO 9001:2015	Variable

Physician Insight & Safety Protocols

“As a General Practitioner experienced in autoimmune diagnostics, I emphasize that the Autoimmune Encephalitis Panel on CSF provides definitive antibody evidence, but results must be interpreted alongside MRI, EEG, and full neurological examination. A positive finding guides immunosuppression; a negative result requires further investigation. Your treating neurologist will integrate all data for personalised care.” — Dr. Ajay Singh, DHA License 36234132

⚠️ Medication Advisory

Do Not Discontinue Prescribed Medications

Abruptly stopping immunosuppressants or anticonvulsants can trigger severe relapse or status epilepticus. Always consult your physician before making any changes.

🚨 Exclusion Criteria & ER Red Flags

Active CNS infection (bacterial/fungal meningitis) must be ruled out before lumbar puncture.
Spinal tap contraindicated if intracranial pressure is elevated or coagulopathy untreated.
Seek emergency care immediately if you develop: sudden severe headache, stiff neck with fever, vision loss, seizures, or worsening confusion after the procedure.

Patient FAQ & Clinical Guidance

1. What does the Autoimmune Encephalitis Panel CSF detect?

First‑line answer: It identifies pathogenic antibodies targeting neuronal surface or synaptic proteins in cerebrospinal fluid, accurately confirming autoimmune encephalitis subtypes.

2. Why is CSF preferred over blood for this test?

First‑line answer: Autoantibodies are produced intrathecally, making CSF the gold standard with significantly higher diagnostic yield than serum.

3. How should I interpret my panel results and next steps?

First‑line answer: A positive result confirms autoimmune encephalitis subtype and guides immunotherapy; a negative result requires clinical correlation with MRI and EEG.

UAE Regulatory & Data Privacy Adherence

Federal Compliance & Patient Data Protection

This test is performed under the regulatory oversight of the Dubai Health Authority (DHA) and complies 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 are encrypted, access‑controlled, and processed in accordance with UAE health‑data governance standards. Clinical safety and informed consent follow Federal Decree‑Law No. 4 of 2016 on Medical Liability.

Clinical & Logistical Metadata

Test Name	Autoimmune Encephalitis Panel – Cerebrospinal Fluid
Price (AED)	3,000 AED
Turnaround Time	Same day (sample received Tue/Fri by 9 AM)
Sample Type / Matrix	Cerebrospinal Fluid (CSF) – Hospital Extraction Only
Methodology Used	Cell‑Based Assay (CBA) + Indirect Immunofluorescence (IFA) + Immunoblot
ICD-10-CM Code	G04.81
LOINC Code	100385-9
DHA Facility License & Laboratory Address	License No. 1143 · Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE · DNA Labs UAE