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Medical information Clinical review pending

Diagnostic Testing

Lead Poisoning Panel Test

The Lead Poisoning Panel Test measures 5-Amino Levulinic Acid (5-ALA) and Lead Blood levels to diagnose lead exposure, a serious condition with potential health consequences. 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.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
24-hour urine collection (10 mL minimum) in a dark-colored container without preservative, shipped frozen. Whole blood (4 mL minimum) collected in a metal-free Royal Blue Top (K2EDTA) tube, shipped refrigerated.
Results
Sample collected on Tuesday or Friday by 9 am; report available the next day. Confirm with the laboratory before booking.
Preparation
If gadolinium or iodine-containing contrast media has been administered, specimen collection should be delayed for 96 hours. Use powderless gloves during specimen collection. Record 24-hour urine volume on the test request form and container.
Test priceKSh 15,000

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 Lead Poisoning 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.

  • ✓Symptoms suggestive of lead poisoning (e.g., abdominal pain, fatigue, cognitive difficulties).
  • ✓Occupational exposure in industries involving lead.
  • ✓Children living in environments with potential lead sources (e.g., older homes with lead paint).
  • ✓Individuals with known risk factors for lead exposure.
  • ✓Monitoring after potential exposure incidents.
02

In plain language

What this test helps you understand

This test helps identify individuals with lead exposure by measuring levels of 5-Amino Levulinic Acid (5-ALA) and Lead in the blood. It aids in the diagnosis of lead poisoning and guides appropriate medical management.
The Lead Poisoning Panel Test is a vital diagnostic tool used to identify lead exposure in individuals. Lead poisoning is a serious health concern that can arise from various sources, such as industrial environments, contaminated water supplies, or certain household products. Early detection through testing is crucial for preventing severe health complications. This test provides a comprehensive assessment by measuring specific markers in the body. Understanding your risk factors and potential exposure is the first step towards protecting your health.
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 →
PreparationIf gadolinium or iodine-containing contrast media has been administered, specimen collection should be delayed for 96 hours. Use powderless gloves during specimen collection. Record 24-hour urine volume on the test request form and container.
Sample24-hour urine collection (10 mL minimum) in a dark-colored container without preservative, shipped frozen. Whole blood (4 mL minimum) collected in a metal-free Royal Blue Top (K2EDTA) tube, shipped refrigerated.
MethodologyConfirm with the laboratory before booking.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
Test results should be interpreted in conjunction with clinical history and other relevant diagnostic information. Certain factors, such as recent contrast media administration, can affect results.
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

Lead poisoning is a serious health condition caused by the accumulation of lead in the body, which can damage various organs and systems.
Individuals working in certain industries, children living in older homes, and those exposed to contaminated sources are at higher risk.
Symptoms can vary but may include abdominal pain, fatigue, headaches, irritability, and developmental delays in children.
Diagnosis typically involves a blood test to measure lead levels, often accompanied by tests like the Lead Poisoning Panel.
Measuring both provides a more comprehensive assessment of lead exposure and its potential effects on the body's metabolic processes.
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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