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Medical information Clinical review pending

Genetic Testing

Filaria RNA Detection Qualitative Test

Detects active filarial infections caused by parasitic worms using Real Time PCR on blood or biopsy samples. Essential for early diagnosis and management in endemic areas.

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
Whole blood (EDTA tube) or Biopsy sample. Confirm specific requirements with the laboratory before booking.
Results
Results typically available via email within 48 hours and via phone within 36 hours. Confirm exact turnaround time with the laboratory before booking.
Preparation
No specific fasting is required. Please inform the laboratory of any medications you are taking. Ensure you sign the consent document.
Test priceKSh 10,880

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 Filaria RNA Detection Qualitative 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.

  • ✓Symptoms suggestive of filariasis (e.g., swelling, fever, abdominal pain)
  • ✓Residence or travel in filariasis-endemic areas
  • ✓History of mosquito bites in endemic regions
  • ✓Screening individuals at high risk of exposure
  • ✓Confirmation of suspected filarial infection
02

In plain language

What this test helps you understand

This test helps identify active filarial infections, guiding appropriate treatment and management to prevent disease progression and complications.
The Filaria RNA Detection Qualitative Test is a diagnostic tool used to identify filarial infections, which are caused by parasitic worms transmitted through mosquito bites. This test is particularly important in regions where filariasis is endemic, as early detection can lead to effective treatment and management of the disease.

This test employs Real Time PCR technology to detect the presence of Filaria RNA in the patient's sample, which can be whole blood or biopsies. The detection of RNA indicates an active infection, allowing for timely medical intervention.

Individuals who should consider the Filaria RNA Detection Qualitative Test include:

* Those experiencing symptoms such as swelling, fever, or abdominal pain. * People living in or traveling to areas where filariasis is common. * Individuals with a history of mosquito bites in endemic regions.

The benefits of this test include:

* Early detection of filarial infections, which can prevent complications. * Accurate diagnosis leading to appropriate treatment options. * Peace of mind for individuals at risk of infection.

Upon receiving your results, it is essential to consult with a healthcare professional to understand the implications of the findings. A positive result indicates an active infection that requires immediate medical attention, while a negative result suggests the absence of the disease.

We have branches across Kenya, making it convenient for you to access our services. Additionally, we offer home sample collection for your comfort. To book the Filaria RNA Detection Qualitative Test, please call or WhatsApp us at +254711564616.
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 fasting is required. Please inform the laboratory of any medications you are taking. Ensure you sign the consent document.
SampleWhole blood (EDTA tube) or Biopsy sample. Confirm specific requirements with the laboratory before booking.
MethodologyReal Time PCR (Polymerase Chain Reaction) for RNA detection.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence of Filaria RNA, indicating an active infection. It may not detect past infections or very low levels of parasites. False negatives can occur if the sample is collected improperly or if the parasite load is below the detection limit. 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

Filariasis is a parasitic disease caused by infection with roundworms of the Filarioidea type, transmitted through mosquito bites.
Early detection allows for timely treatment, which can prevent the progression of the disease and reduce the risk of long-term complications.
The test can be performed on a whole blood sample collected in an EDTA tube or a biopsy sample. Please confirm the required sample type with the laboratory.
The Real Time PCR method used is highly sensitive and specific for detecting Filaria RNA, providing an accurate diagnosis of active infection.
If you receive a positive result, it is crucial to consult with your healthcare provider immediately to discuss treatment options and management.
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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