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Cytogenetics

Immunophenotyping by Flow Cytometry Leukemia Lymphoma Diagnostic Panel Chronic Lymphoproliferative Disorders T B Cell Test

Immunophenotyping by Flow Cytometry helps diagnose Chronic Lymphoproliferative Disorders like leukemia and lymphoma by analyzing blood or bone marrow cells. This test identifies specific cell types to 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
3 mL (2 mL min.) whole blood in 1 Lavender Top (EDTA) tube AND 1 Green Top (Sodium Heparin) tube. OR 2 mL (1 mL min.) bone marrow in 1 Green Top (Sodium Heparin) tube AND aspirate smear.
Results
Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required. Confirm with the laboratory before booking.
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 Immunophenotyping by Flow Cytometry Leukemia Lymphoma Diagnostic Panel Chronic Lymphoproliferative Disorders T B Cell 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.

  • ✓Suspected leukemia or lymphoma
  • ✓Evaluation of unexplained lymphocytosis
  • ✓Monitoring known hematological malignancies
  • ✓Diagnosis of Chronic Lymphoproliferative Disorders
  • ✓Assessment of disease progression
  • ✓Guiding treatment strategies
02

In plain language

What this test helps you understand

Diagnosis and classification of Chronic Lymphoproliferative Disorders (CLPD), including leukemia and lymphoma. Monitoring disease progression and response to therapy. Guiding treatment decisions based on specific cell characteristics.
The Immunophenotyping by Flow Cytometry test is a key diagnostic tool for evaluating Chronic Lymphoproliferative Disorders (CLPD), which include conditions like leukemia and lymphoma. It uses a technique called flow cytometry to examine the characteristics of cells in your blood or bone marrow. This analysis helps identify abnormal cell populations that could indicate a blood cancer.

This test measures the types and proportions of specific cells present. By looking at the 'immunophenotype' – the specific markers on the surface of cells – healthcare providers can better understand the nature of the disorder and develop appropriate treatment strategies.

Individuals experiencing symptoms like persistent fatigue, unexplained weight loss, frequent infections, or swollen lymph nodes may be advised to consider this test. People with risk factors, such as a family history of blood cancers, might also benefit from discussing this test with their doctor.

Early detection of hematological malignancies is crucial. This test provides vital information for oncologists and hematologists to guide treatment decisions, monitor how the disease is progressing, and develop personalized care plans.

Results will be interpreted by a specialist, such as a hematologist or oncologist. They will explain the findings and discuss the implications for your health and potential next steps in management. It's important to have a detailed discussion with your doctor to fully understand your results.
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 →
PreparationNo specific patient preparation is required. Confirm with the laboratory before booking.
Sample3 mL (2 mL min.) whole blood in 1 Lavender Top (EDTA) tube AND 1 Green Top (Sodium Heparin) tube. OR 2 mL (1 mL min.) bone marrow in 1 Green Top (Sodium Heparin) tube AND aspirate smear.
MethodologyFlow Cytometry
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
Test results must be interpreted in the context of the patient's clinical presentation, medical history, and other laboratory findings. The test may not detect all types of hematological malignancies or subtle abnormalities. 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

It is a laboratory technique that analyzes the characteristics of cells, particularly blood or bone marrow cells, to help diagnose and classify diseases like leukemia and lymphoma.
It helps identify specific types of abnormal cells involved in Chronic Lymphoproliferative Disorders, which is crucial for accurate diagnosis and determining the best treatment plan.
The test typically requires a blood sample collected in specific tubes (Lavender and Green Top) or a bone marrow sample.
Turnaround time varies. Please contact the laboratory for specific details regarding this test.
A qualified specialist, such as a hematologist or oncologist, will interpret the results and discuss them with your referring physician.
This test is a key tool used by doctors to help diagnose certain types of blood cancers, but the diagnosis is based on a combination of test results, clinical findings, and medical history.
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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