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Medical information Clinical review pending

Neurology

Ganglioside GD1b Antibody IgM Test

The Ganglioside GD1b Antibody IgM Test helps diagnose certain autoimmune neurological disorders by detecting specific antibodies in your blood. It is used to investigate symptoms affecting the nervous system.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
2 mL (minimum 1 mL) serum collected in one SST tube.
Results
Results are typically available within 2 to 3 weeks after sample collection. Confirm with the laboratory before booking.
Preparation
Overnight fasting is preferred. A duly filled Test Send Out Consent Form (Form 35) is mandatory.
Test priceKSh 22,000

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the Ganglioside GD1b Antibody IgM Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Investigating unexplained weakness or numbness
  • ✓Diagnosing potential Guillain-Barré syndrome
  • ✓Evaluating symptoms of nerve damage
  • ✓Assessing autoimmune conditions affecting the nervous system
  • ✓Monitoring neurological disorders
02

In plain language

What this test helps you understand

This test aids in the diagnosis and management of autoimmune neurological disorders by detecting specific antibodies linked to nerve dysfunction.
The Ganglioside GD1b Antibody IgM Test is a specialized diagnostic tool used to identify the presence of antibodies associated with certain autoimmune neurological disorders. This test is crucial for neurologists in determining the underlying causes of various symptoms affecting the nervous system.

This test detects the presence of IgM antibodies against Ganglioside GD1b, which are indicative of autoimmune responses that may impact neurological function. A positive result can suggest the presence of disorders such as Guillain-Barré syndrome, among others.

Individuals experiencing the following symptoms or risk factors may benefit from the Ganglioside GD1b Antibody IgM Test:

- Weakness or numbness in limbs - Difficulty walking or maintaining balance - Symptoms of nerve damage or dysfunction - History of autoimmune diseases

Taking the Ganglioside GD1b Antibody IgM Test can provide several benefits, including:

- Early detection of potential autoimmune neurological disorders. - Guidance for appropriate treatment plans based on test results. - Improved patient outcomes through timely intervention.

Results from the Ganglioside GD1b Antibody IgM Test will be available within 2 to 3 weeks after sample collection. A positive result may indicate an autoimmune response, while a negative result can help rule out specific conditions. It is essential to discuss your results with a healthcare professional for accurate interpretation and further recommendations.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationOvernight fasting is preferred. A duly filled Test Send Out Consent Form (Form 35) is mandatory.
Sample2 mL (minimum 1 mL) serum collected in one SST tube.
MethodologyConfirm with the laboratory before booking.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects IgM antibodies against GD1b. Results must be interpreted alongside clinical findings and other relevant tests. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

This test detects IgM antibodies against Ganglioside GD1b, which can indicate an autoimmune response affecting the nervous system.
Individuals with symptoms like limb weakness, numbness, balance problems, or a history of autoimmune diseases may be recommended this test.
Results are typically available within 2 to 3 weeks after the sample is received by the laboratory.
A blood sample (serum) is required for this test.
Overnight fasting is preferred, but please confirm specific requirements with your doctor or the laboratory.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

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09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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