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Medical information Clinical review pending

Cytogenetics

Synovial Sarcoma SS18

The Synovial Sarcoma SS18 test helps detect genetic markers associated with Synovial Sarcoma, a rare cancer. This test uses FISH methodology on tumor tissue.

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
Tumor tissue sample (biopsy or surgical resection). Confirm specific requirements with the laboratory before booking.
Results
Results are typically available within 7-8 days. Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required for this test. The sample is typically obtained via biopsy or surgery.
Test priceKSh 18,000

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 Synovial Sarcoma SS18 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.

  • ✓Suspicion of Synovial Sarcoma based on clinical presentation
  • ✓Evaluation of soft tissue or joint masses
  • ✓Confirmation of diagnosis in suspected cases
  • ✓Assisting in treatment planning for sarcoma
  • ✓Monitoring for specific genetic markers in oncology
02

In plain language

What this test helps you understand

This test aids in the diagnosis of Synovial Sarcoma by detecting the characteristic SS18 gene fusion. It helps confirm the diagnosis, guiding appropriate treatment strategies and prognosis.
The Synovial Sarcoma SS18 test is a specialized diagnostic procedure used to identify genetic markers linked to Synovial Sarcoma. This is a rare and aggressive cancer primarily affecting joints and soft tissues. Accurate diagnosis is vital for determining appropriate treatment and managing the condition effectively.

This test utilizes Fluorescence In Situ Hybridization (FISH) technology to analyze tumor tissue samples. It specifically looks for the SS18 gene fusion, a characteristic genetic abnormality found in Synovial Sarcoma.

Patients experiencing persistent swelling, joint pain, or unusual soft tissue masses may be advised to consider this test. Individuals with a family history of cancer or those with previous cancer diagnoses might also benefit from this diagnostic tool.

Benefits of this test include aiding in the early and accurate diagnosis of Synovial Sarcoma, guiding treatment decisions, and potentially monitoring treatment effectiveness. Discussing the results with your doctor is essential for understanding their implications and planning next steps.
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 for this test. The sample is typically obtained via biopsy or surgery.
SampleTumor tissue sample (biopsy or surgical resection). Confirm specific requirements with the laboratory before booking.
MethodologyFluorescence In Situ Hybridization (FISH) on tumor tissue.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence or absence of the SS18 gene fusion. It may not detect all types of Synovial Sarcoma or other related cancers. Results must be interpreted in the context of clinical findings and other diagnostic 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

Synovial Sarcoma is a rare type of cancer that usually develops near joints and tendons, often in the arms or legs. It can also occur in other parts of the body.
The test detects a specific genetic change called the SS18 gene fusion, which is commonly found in Synovial Sarcoma cells.
A positive result indicates the presence of the SS18 gene fusion, strongly suggesting Synovial Sarcoma, but it must be interpreted by a doctor alongside clinical information and other tests.
The sample required for this test is typically a piece of tumor tissue obtained through a biopsy or surgical removal.
Results are generally available within 7-8 days, but this can vary. Confirm the current 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.

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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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