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Medical information Clinical review pending

Genetic Testing

CTLA4 Gene Lymphoproliferative Syndrome Autoimmune Type 5 Genetic Test

This genetic test identifies mutations in the CTLA4 gene, which can be associated with autoimmune disorders. It helps understand genetic predispositions and guide treatment.

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
Blood sample (EDTA tube), extracted DNA, or one drop of blood on an FTA card.
Results
Approximately 3 to 4 weeks. Confirm with the laboratory before booking.
Preparation
Confirm with the laboratory before booking. Genetic counselling prior to testing is recommended to discuss clinical history and family history.
Test priceKSh 40,000

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 CTLA4 Gene Lymphoproliferative Syndrome Autoimmune Type 5 Genetic 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.

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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.

  • ✓Family history of autoimmune diseases
  • ✓Symptoms suggestive of autoimmune disorders (e.g., unexplained fatigue, joint pain)
  • ✓Evaluation of lymphoproliferative syndromes
  • ✓Understanding genetic predisposition to autoimmune conditions
02

In plain language

What this test helps you understand

Identifies genetic mutations in the CTLA4 gene associated with autoimmune disorders. Helps assess individual risk and inform clinical management.
This genetic test assesses for mutations in the CTLA4 gene, which plays a role in regulating the immune system. Understanding variations in this gene can provide insights into a person's risk for certain autoimmune conditions. This test is performed using Next Generation Sequencing (NGS) technology on a DNA sample. It is particularly relevant for individuals with a family history of autoimmune diseases or those experiencing symptoms suggestive of such conditions. Results can help inform diagnosis and potential treatment strategies, often in conjunction with clinical evaluation and other tests. Discussing the results with a healthcare provider or genetic counsellor is essential for understanding their implications.
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 →
PreparationConfirm with the laboratory before booking. Genetic counselling prior to testing is recommended to discuss clinical history and family history.
SampleBlood sample (EDTA tube), extracted DNA, or one drop of blood on an FTA card.
MethodologyNext Generation Sequencing (NGS) analysis of the CTLA4 gene.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects specific mutations in the CTLA4 gene but does not rule out other genetic or environmental factors contributing to autoimmune disorders. A negative result does not guarantee the absence of the condition. Interpretation requires clinical correlation.
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

The CTLA4 gene provides instructions for making a protein that helps regulate the immune system. Variations in this gene can affect immune responses.
Individuals with a family history of autoimmune diseases, those experiencing symptoms like persistent fatigue or joint pain, or those being evaluated for lymphoproliferative syndromes may be candidates.
A sample can be collected as a blood draw, using previously extracted DNA, or via a single drop of blood on a special card (FTA card).
Results will indicate if specific mutations in the CTLA4 gene were detected. A healthcare provider or genetic counsellor will interpret these results in the context of your clinical picture.
Yes, genetic counselling before testing is recommended to discuss your personal and family medical history, understand the test's implications, and interpret the results effectively.
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.

Explore partnerships
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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