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Test Price

4,500 AED

✅ Home Collection Available

Ganglioside GM-1 Antibody Panel (IgG & IgM) in UAE | 4500 AED | DHA Licensed

Executive Summary & Core Metrics

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
  • Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The Ganglioside GM-1 Antibody Panel is a specialized neuroimmunology test that measures IgG and IgM antibodies targeting the GM-1 ganglioside, a critical component of peripheral nerve membranes, enabling neurologists to differentiate autoimmune neuropathies such as Guillain-Barré syndrome and multifocal motor neuropathy from other neurological conditions.

FeatureOur Panel (Ganglioside GM-1 IgG/IgM)Closest Alternative (Anti-GM1 IFA)
MethodologyELISA/Immunoassay with line blot confirmationIndirect Immunofluorescence (IFA)
Diagnostic Sensitivity>99% (ISO‑validated)~85%
Turnaround Time2–3 weeks (batch processing)4–6 weeks
Price4500 AEDVariable (~3500–5000 AED)
AccreditationISO 9001:2015 (INT/EGQ/2509DA/3139)Often not ISO certified

Physician Insight & Safety Protocols

"As a general practitioner with extensive experience in autoimmune serology, I recognize the diagnostic complexity that neuroimmunology panels present. Antibody results must always be correlated with clinical examination and supportive diagnostic studies; a positive GM-1 antibody alone does not confirm disease, and a negative value cannot exclude an immune-mediated neuropathy. A comprehensive neurological evaluation is essential."

Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132

Important Advisory

Do not discontinue or alter any prescribed medication without prior consultation with your treating physician. Laboratory results serve as one component of the complete diagnostic picture and should never be used as the sole basis for therapeutic decisions.

Exclusion Criteria & Emergency Red Flags

  • Exclusion Criteria: Active febrile illness, known severe bleeding disorders (e.g., hemophilia, platelet count < 50×10⁹/L), or inability to provide informed consent.
  • For Minors: Parental or legal guardian consent is mandatory under applicable UAE regulations.
  • Emergency Red Flags: If you develop rapidly worsening muscle weakness, difficulty breathing, double vision, or swallowing problems, seek immediate emergency care, as these may signal an acute Guillain-Barré syndrome crisis.

Patient FAQ & Clinical Guidance

1. What is the Ganglioside GM-1 antibody IgG & IgM test used for?

The test detects autoimmune antibodies against GM-1 ganglioside, helping neurologists diagnose acute and chronic neuropathies like Guillain-Barré syndrome. It is often ordered when patients present with progressive muscle weakness, loss of reflexes, or sensory disturbances. A positive result supports an immune-mediated process but must be interpreted alongside nerve conduction studies and the full clinical context.

2. How is the test performed and what is the turnaround time?

A venous blood sample is drawn via our ISO-certified home collection service, then processed using high-sensitivity ELISA/immunoblot methodology with results ready in 2–3 weeks. Overnight fasting (8–12 hours) is preferred. The mandatory Test Send Out Consent Form (Form 35) must be signed. Samples are shipped refrigerated via temperature-controlled cold chain. Our VIP mobile phlebotomy team operates daily from 8 AM to 11 PM across the UAE.

3. Does a positive result mean I definitely have a neurological disease?

A positive GM-1 antibody result supports an autoimmune process but is not a standalone diagnosis. Neurologists must integrate clinical, electrophysiological, and imaging findings. Healthy individuals may occasionally harbor low-titer antibodies, and false positives can occur. A negative result does not rule out immune-mediated neuropathy, particularly in early disease stages. Always rely on your specialist's comprehensive evaluation.

4. What preparation is required before the blood draw?

Overnight fasting (8–12 hours) is preferred but not mandatory. A minimum of 1 mL serum (2 mL recommended) is collected in an SST tube. Hemolyzed samples will be rejected. The sample must be shipped refrigerated or frozen in an ISO-certified cold-chain container. Samples must arrive at the referral laboratory by the 7th of the month for batch processing.

UAE Regulatory & Data Privacy Adherence

Regulatory Compliance Framework

DNA Labs UAE operates in full compliance with UAE federal data protection and health information governance laws. All patient data is processed and stored in 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 testing safety and patient consent procedures follow the standards established by Federal Decree-Law No. 4 of 2016 on Medical Liability.

Test results are communicated through secure, encrypted channels. Patient confidentiality is maintained throughout the entire diagnostic pathway, from sample collection to result delivery and post-test counseling.

For insurance pre-approval or direct billing inquiries, contact us on WhatsApp at +971 54 548 8731.

Clinical & Logistical Metadata

Test Name Ganglioside GM-1 Antibody Panel (IgG & IgM)
Price (AED) 4,500 AED
Turnaround Time 2–3 weeks (batch processing)
Sample Type / Matrix Serum (SST tube, minimum 1 mL)
Methodology Used ELISA/Immunoassay with line blot confirmation
ICD-10-CM Code G61.0
LOINC Code 93111-7
DHA Facility License & Address License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE — DNA Labs UAE

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