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Medical information Clinical review pending

Cytogenetics

FISH Eosinophilic Leukemia Panel Test

The FISH Eosinophilic Leukemia Panel Test uses advanced genetic technology (FISH) to detect specific abnormalities linked to eosinophilic leukemia, aiding in diagnosis and treatment planning.

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
5 mL (3 mL minimum) whole blood OR 4 mL (2 mL minimum) Bone Marrow collected in 2 Green Top (Sodium Heparin) tubes.
Results
Results are typically available within four working days. Confirm with the laboratory before booking.
Preparation
Confirm with the laboratory before booking. Ensure a duly filled Chromosome & FISH analysis Requisition Form (Form 17) is provided with the sample.
Test priceKSh 34,000

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 FISH Eosinophilic Leukemia Panel 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.

  • ✓Suspicion of eosinophilic leukemia.
  • ✓Diagnosis of hematological malignancies.
  • ✓Identification of specific genetic markers (PDGFRA, PDGFRB, FGFR1, CBFB).
  • ✓Guiding treatment strategies for leukemia.
  • ✓Monitoring disease progression or response to therapy.
02

In plain language

What this test helps you understand

This test helps identify specific genetic abnormalities associated with eosinophilic leukemia, aiding in diagnosis, prognosis, and guiding treatment decisions.
The FISH Eosinophilic Leukemia Panel Test is a specialized diagnostic tool designed to identify specific genetic changes associated with eosinophilic leukemia. This test utilizes Fluorescence In Situ Hybridization (FISH) technology, which allows for the visualization of specific genes or chromosomes within cells. It is a crucial part of the diagnostic process for patients suspected of having certain types of leukemia. The test analyzes key genetic markers, including PDGFRA, PDGFRB, FGFR1, and CBFB (inv16), which are known to be involved in the development of eosinophilic leukemia. Understanding these genetic alterations helps healthcare providers make accurate diagnoses and tailor treatment strategies effectively. This test is particularly important for hematologists and oncologists managing patients with complex blood disorders.
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. Ensure a duly filled Chromosome & FISH analysis Requisition Form (Form 17) is provided with the sample.
Sample5 mL (3 mL minimum) whole blood OR 4 mL (2 mL minimum) Bone Marrow collected in 2 Green Top (Sodium Heparin) tubes.
MethodologyFluorescence In Situ Hybridization (FISH)
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects specific genetic abnormalities but may not identify all possible genetic changes associated with leukemia. Results must be interpreted in the context of the patient's clinical presentation and other laboratory findings. 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

Eosinophilic leukemia is a type of blood cancer characterized by an overproduction of eosinophils, a type of white blood cell. This test helps identify specific genetic changes associated with this condition.
FISH (Fluorescence In Situ Hybridization) is a laboratory technique that uses fluorescent probes to detect specific DNA sequences on chromosomes. It helps identify genetic abnormalities within cells.
The sample required is either a blood sample or a bone marrow sample, collected in specific tubes as outlined in the specimen requirements.
The turnaround time is typically four working days, but this can vary. Your healthcare provider will receive the results.
Yes, DNA Labs Kenya offers home sample collection services for your convenience. Please contact us to arrange this.
Your doctor will interpret the results in the context of your overall health and clinical picture. The test identifies specific genetic markers relevant to eosinophilic leukemia.
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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