Skip to main content
Medical information Clinical review pending

Cytogenetics

FISH T 1517 OR LSI PMLRARA Test

The FISH T 1517 OR LSI PMLRARA Test detects specific genetic changes linked to leukemia, aiding in diagnosis and treatment planning. Confirm with the laboratory before booking.

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.

Ask a question
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
No specific patient preparation is required. Ensure the sample is collected correctly as per laboratory guidelines.
Test priceKSh 12,000

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 T 1517 OR LSI PMLRARA 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.

+254

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 acute promyelocytic leukemia (APL)
  • ✓Diagnosis of leukemia
  • ✓Monitoring leukemia treatment response
  • ✓Identifying specific chromosomal abnormalities in blood or bone marrow cells
  • ✓Patients with symptoms suggestive of leukemia
02

In plain language

What this test helps you understand

This test helps identify specific genetic abnormalities associated with leukemia, particularly the PML-RARA fusion gene, which aids in diagnosis, prognosis, and guiding treatment decisions.
The FISH T 1517 OR LSI PMLRARA Test is a specialized diagnostic procedure used to identify specific genetic abnormalities associated with certain types of leukemia. It utilizes Fluorescence In Situ Hybridization (FISH) technology to visualize genetic markers within cells. This information is vital for healthcare providers, particularly oncologists and hematologists, to accurately diagnose leukemia and develop appropriate treatment strategies.

This test specifically looks for chromosomal changes, including the PML-RARA fusion gene, which is often found in acute promyelocytic leukemia (APL). Identifying these genetic alterations helps doctors understand the specific type of leukemia and choose the most effective therapies.

Consider discussing this test with your doctor if you have symptoms suggestive of leukemia, a family history of the disease, or are currently undergoing leukemia treatment and require monitoring.
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. Ensure the sample is collected correctly as per laboratory guidelines.
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 types of leukemia or all genetic changes. Results must be interpreted in conjunction with clinical findings and other laboratory tests. 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

This test uses FISH technology to detect specific genetic changes, like the PML-RARA fusion gene, often associated with acute promyelocytic leukemia (APL).
It helps doctors diagnose leukemia accurately, understand its specific type, and choose the most effective treatment plan.
Individuals with symptoms of leukemia, a family history of leukemia, or those undergoing leukemia treatment may be advised to take this test by their doctor.
The test requires either a whole blood sample or a bone marrow sample collected in specific tubes.
Results are generally available within four working days, but confirm the exact turnaround time 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.

Keep exploring

Related tests

View all tests →
Chat on WhatsApp