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DNA LabsKenya
Medical information Clinical review pending

Diagnostic Testing

Small Biopsy (1) Punch Biopsy, GI Biopsy, Gall Bladder, Appendix, D&C, Bone Marrow

Tissue analysis test for diagnosing conditions in various organs like the GI tract, gall bladder, appendix, and bone marrow. Helps detect abnormalities and genetic conditions.

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
Tissue sample obtained via biopsy (e.g., punch biopsy, GI biopsy, gall bladder, appendix, D&C, bone marrow). Confirm specific sample type required with the laboratory before booking.
Results
Results are typically available within 3 days. Confirm exact turnaround time with the laboratory before booking.
Preparation
Follow your doctor's specific instructions. Generally, no special preparation is needed, but inform your doctor about all medications you are taking, including blood thinners. Confirm preparation details with the laboratory.
Test priceKSh 3,900

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 Small Biopsy (1) Punch Biopsy, GI Biopsy, Gall Bladder, Appendix, D&C, Bone Marrow 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.

  • ✓Unexplained pain or discomfort
  • ✓Gastrointestinal symptoms (e.g., bleeding, persistent pain, changes in bowel habits)
  • ✓Suspicious growths or lesions detected during imaging
  • ✓Investigation of potential infections or inflammation
  • ✓Diagnosis of certain genetic disorders
  • ✓Monitoring response to treatment for specific conditions
02

In plain language

What this test helps you understand

This test is used to diagnose a wide range of conditions, including inflammatory diseases, infections, cancers, and genetic disorders affecting the tissues sampled. It helps determine the nature of abnormal growths and guides treatment decisions.
This test involves the analysis of small tissue samples obtained from different parts of the body, such as the gastrointestinal tract, gall bladder, appendix, or bone marrow. A qualified General Surgeon performs the biopsy, and the collected tissue is examined under a microscope by a histopathologist. This detailed examination helps identify cellular structures and compositions, revealing potential abnormalities, diseases, or genetic conditions. The results provide crucial information for accurate diagnosis and effective treatment planning.
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 →
PreparationFollow your doctor's specific instructions. Generally, no special preparation is needed, but inform your doctor about all medications you are taking, including blood thinners. Confirm preparation details with the laboratory.
SampleTissue sample obtained via biopsy (e.g., punch biopsy, GI biopsy, gall bladder, appendix, D&C, bone marrow). Confirm specific sample type required with the laboratory before booking.
MethodologyHistopathology: Microscopic examination of stained tissue sections by a pathologist.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
The accuracy of the test depends on the quality and representativeness of the tissue sample obtained. Results may sometimes be inconclusive, requiring further investigation or repeat biopsy. This test does not provide information about all possible conditions.
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

A biopsy is a procedure where a small sample of tissue is removed from the body for examination under a microscope.
Pain levels vary depending on the biopsy location and the individual. Local anaesthesia is often used to minimize discomfort. Discuss pain management with your doctor.
A pathologist examines the tissue sample and provides a report. Your doctor will discuss the findings with you and explain their significance.
You may need to follow up with your doctor to discuss the results and determine the next steps in your care, which could include further tests or treatment.
Results are typically provided to your referring doctor, who will then discuss them with you. Confirm the reporting process with 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.

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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