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Genetic Testing

Molecular Karyotyping for Amniotic Fluid Test

Molecular Karyotyping for Amniotic Fluid Test is an advanced genetic test for expectant mothers to detect chromosomal abnormalities in the fetus. Provides crucial information for informed pregnancy decisions.

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
Amniotic fluid sample.
Results
Results are typically available within 7-9 days. Confirm with the laboratory before booking.
Preparation
This test is typically performed during the second trimester of pregnancy (around 15-20 weeks). An amniocentesis procedure is required to collect the sample. Discuss preparation details with your healthcare provider.
Test priceKSh 36,000

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 Molecular Karyotyping for 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.

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.

  • ✓Advanced maternal age (over 35)
  • ✓Abnormal prenatal ultrasound findings
  • ✓Family history of chromosomal abnormalities
  • ✓Previous child with a chromosomal abnormality
  • ✓Known parental carrier status for genetic conditions
  • ✓Abnormal prenatal screening results
02

In plain language

What this test helps you understand

Detects chromosomal abnormalities (deletions, duplications, aneuploidies) in a fetus using amniotic fluid, aiding in prenatal diagnosis and management.
Molecular Karyotyping for Amniotic Fluid Test

This test is an advanced genetic method used to analyze chromosomal abnormalities in a fetus during pregnancy. It is particularly recommended for expectant mothers who may be at higher risk for genetic disorders.

What the Test Measures

The test identifies chromosomal abnormalities like deletions, duplications, and other genetic anomalies that could impact fetal development. By examining genetic material from amniotic fluid, healthcare providers can identify potential risks for conditions such as Down syndrome and other genetic disorders.

Who Should Consider This Test?

Expectant mothers, especially those who:

- Are over the age of 35 - Have a family history of genetic disorders - Have abnormal ultrasound findings - Are known carriers of genetic conditions

This test is recommended for those seeking a deeper understanding of their unborn child's genetic health.

Benefits of Taking the Test

- Early detection of potential genetic issues - Supports informed decision-making regarding pregnancy management - Provides peace of mind for expectant parents - Guides further testing or interventions if necessary

Understanding Your Results

Results are typically available within 7-9 days. A genetic counselor or gynecologist will discuss the findings with you, explaining their implications for the pregnancy and potential next steps.

Branches Across Kenya

We have branches in major cities including Nairobi, Mombasa, and Kisumu. Home sample collection is also available for convenience.
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 →
PreparationThis test is typically performed during the second trimester of pregnancy (around 15-20 weeks). An amniocentesis procedure is required to collect the sample. Discuss preparation details with your healthcare provider.
SampleAmniotic fluid sample.
MethodologyMolecular techniques, such as chromosomal microarray analysis (CMA) or quantitative PCR (qPCR), are used to analyze the DNA extracted from the amniotic fluid sample.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test analyzes chromosomes but may not detect all types of genetic mutations or single-gene disorders. 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

Amniocentesis is a medical procedure used to collect a sample of amniotic fluid surrounding the fetus during pregnancy. This fluid contains fetal cells that can be tested.
This test is typically performed during the second trimester of pregnancy, usually between 15 and 20 weeks gestation.
The test results will indicate whether any chromosomal abnormalities were detected in the fetal cells. Your doctor or a genetic counselor will explain the results.
This test focuses on chromosomal abnormalities. It may not detect all types of genetic conditions, such as single-gene disorders. Discuss specific concerns with your doctor.
Amniocentesis carries a small risk of complications. Your healthcare provider will discuss the risks and benefits of the procedure with you.
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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