Medical information Clinical review pending

Gynecological Testing

Acetylcholinesterase Amniotic Fluid Test

The Acetylcholinesterase Amniotic Fluid Test helps detect potential fetal abnormalities during pregnancy. This prenatal diagnostic tool measures enzyme levels in amniotic fluid.

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: 3 ml (1 mL minimum) of amniotic fluid in a sterile screw-capped vial.
Results: Results are typically available within 2-3 weeks. Confirm exact turnaround time with the laboratory before booking.
Preparation: Sample collection should ideally occur between 13 and 24 weeks of gestation. Avoid blood contamination during collection. Ensure the Test Request Form includes gestational age, collection date, clinical indications, and AFP/MoM results if available. A completed Test Send Out Consent Form (Form 35) is required.

Test priceKSh 26,000

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 Acetylcholinesterase Amniotic Fluid 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.

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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.

✓Abnormal results from previous prenatal screenings
✓Family history of genetic disorders
✓Advanced maternal age
✓Previous pregnancies with complications
✓Abnormalities detected during ultrasound
✓Unusual fetal movements

In plain language

What this test helps you understand

This test aids in the prenatal diagnosis of certain fetal conditions, particularly neural tube defects, by measuring acetylcholinesterase levels in amniotic fluid.

The Acetylcholinesterase Amniotic Fluid Test is a diagnostic tool used during pregnancy to assess fetal health and identify potential abnormalities. It measures the concentration of the acetylcholinesterase enzyme in the amniotic fluid surrounding the baby. Elevated levels can indicate certain fetal conditions, such as neural tube defects. This test is particularly important for expectant mothers who may be at higher risk for genetic disorders or other complications. Early detection allows for informed decision-making and appropriate medical guidance. Discuss with your healthcare provider if this test is right for you.

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.

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A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

Speak with us

We check the test and answer your questions before collection.

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.

Understand your report

A counselor helps you understand the result and the next steps.

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 →

PreparationSample collection should ideally occur between 13 and 24 weeks of gestation. Avoid blood contamination during collection. Ensure the Test Request Form includes gestational age, collection date, clinical indications, and AFP/MoM results if available. A completed Test Send Out Consent Form (Form 35) is required.

Sample3 ml (1 mL minimum) of amniotic fluid in a sterile screw-capped vial.

MethodologyEnzymatic assay to measure acetylcholinesterase concentration in amniotic fluid. Confirm specific methodology with the laboratory before booking.

PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.

This test measures acetylcholinesterase levels and may indicate the presence of certain conditions, but it is not a definitive diagnosis for all fetal abnormalities. Further testing may be required. Confirm specific limitations with the laboratory before booking.

Read your report

What common result terms mean

TermPlain-language meaning

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.

Questions people ask

Frequently asked questions

This test measures acetylcholinesterase levels in amniotic fluid, which can help detect certain fetal abnormalities, particularly neural tube defects.

The sample is typically collected between 13 and 24 weeks of gestation for optimal results.

The sample is amniotic fluid collected via amniocentesis, a procedure performed by a healthcare professional.

Your doctor will interpret the results. Elevated levels may indicate a need for further investigation or consultation with a specialist.

Insurance coverage varies. Please check with your insurance provider regarding coverage for this specific test.

You can book the test by calling or WhatsApping us at +254711564616. You can also visit one of our branches.

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

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Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

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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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