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Medical information Clinical review pending

Haematology Testing

Bone Marrow Examination Panel 2 Test

The Bone Marrow Examination Panel 2 Test evaluates bone marrow health and blood cell production. It helps diagnose conditions like leukemia, anemia, and myelodysplastic syndromes. Essential for unexplained anemia, recurrent infections, or bleeding disorders.

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 (1 mL min.) Bone Marrow Aspirate in 1 Lavender Top (EDTA) tube, 4 Bone Marrow Aspirate Smears (air-dried and fixed in 100% Methanol for 30 minutes), 4 mL (2 mL min) whole blood in 1 Lavender Top (EDTA) tube, 2 peripheral blood smears (air-dried and fixed in 100% Methanol for 30 minutes). A Bone Marrow Trephine biopsy in 10% formal saline is also required. A duly filled Bone Marrow Examination Requisition Form (Form 14) is mandatory.
Results
Confirm with the laboratory before booking.
Preparation
Confirm with the laboratory before booking. Specific instructions regarding fasting or medication adjustments may be provided.
Test priceKSh 6,000

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 Bone Marrow Examination Panel 2 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.

  • ✓Unexplained anemia
  • ✓Recurrent infections
  • ✓Bleeding disorders
  • ✓Fatigue or weakness
  • ✓Suspected leukemia or lymphoma
  • ✓Monitoring response to chemotherapy
  • ✓Evaluation of pancytopenia
  • ✓Family history of blood disorders
02

In plain language

What this test helps you understand

This test provides crucial information for diagnosing and monitoring various blood disorders, including leukemia, anemia, myelodysplastic syndromes, and other conditions affecting blood cell production.
The Bone Marrow Examination Panel 2 Test is a vital diagnostic procedure used to evaluate the health of bone marrow and the production of blood cells. Bone marrow is the spongy tissue found in the center of bones, responsible for producing red blood cells, white blood cells, and platelets. This test is crucial for detecting various hematopoietic disorders, such as leukemia, anemia, and myelodysplastic syndromes.

This comprehensive test includes microscopy of bone marrow aspirate and peripheral blood, special stains, a complete blood count (CBC), and histopathology. It provides a detailed look at the cells within the bone marrow and their development.

Patients experiencing symptoms like unexplained anemia, recurrent infections, bleeding disorders, fatigue, or weakness should consider this test. Additionally, individuals with a family history of blood disorders or those undergoing chemotherapy may benefit from this evaluation.
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. Specific instructions regarding fasting or medication adjustments may be provided.
Sample2 mL (1 mL min.) Bone Marrow Aspirate in 1 Lavender Top (EDTA) tube, 4 Bone Marrow Aspirate Smears (air-dried and fixed in 100% Methanol for 30 minutes), 4 mL (2 mL min) whole blood in 1 Lavender Top (EDTA) tube, 2 peripheral blood smears (air-dried and fixed in 100% Methanol for 30 minutes). A Bone Marrow Trephine biopsy in 10% formal saline is also required. A duly filled Bone Marrow Examination Requisition Form (Form 14) is mandatory.
MethodologyThe panel includes various techniques such as microscopy of bone marrow aspirate and peripheral blood smears, special stains (e.g., cytochemical stains), complete blood count (CBC) analysis, and histopathological examination of the bone marrow trephine biopsy.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
The test results are dependent on the quality of the sample collected and processed. Certain conditions may not be detectable with this panel alone. Interpretation requires correlation with clinical findings and other laboratory tests.
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

Bone marrow is the soft, spongy tissue inside your bones. It's responsible for producing blood cells: red blood cells (carry oxygen), white blood cells (fight infection), and platelets (help blood clot).
This test helps doctors understand if your bone marrow is working correctly and producing healthy blood cells. It's used to diagnose conditions like anemia, leukemia, and other blood disorders.
The test involves collecting samples of bone marrow (aspirate and biopsy) and blood. These samples are then examined under a microscope and analyzed in the laboratory.
Please confirm specific preparation instructions with the laboratory before your appointment. You may be asked to stop certain medications or fast.
Collecting bone marrow samples can cause brief discomfort or pain. Local anesthesia is typically used to minimize this.
Turnaround time varies. Please confirm the expected timeframe with the laboratory before booking.
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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