Kenya Chromosomal Analysis (Karyotyping)

Karyotyping, also known as chromosomal analysis, is a laboratory test that evaluates the number and structure of chromosomes in a person’s cells. It helps detect genetic abnormalities that may affect development, fertility, pregnancy, or overall health. This test is essential for diagnosing chromosomal disorders, identifying causes of infertility or miscarriage, and confirming prenatal abnormalities.

Our Karyotyping Services

Standard Karyotype (Blood)

For children and adults and is indicated for:

Developmental delays

Congenital abnormalities

Disorders of sex development

Suspected genetic syndromes

Prenatal Karyotype

Performed during pregnancy using amniotic fluid or chorionic villus sampling (CVS) and is recommended for:

Abnormal ultrasound findings

Advanced maternal age

Abnormal NIPT results

Suspected genetic syndromes

Infertility & Recurrent Miscarriage Testing

For couples experiencing reproductive challenges and helps to detect the following:

Balanced translocations

Chromosomal rearrangements

Sex chromosome abnormalities

Guide future pregnancy planning

Miscarriage Analysis

Analysis of pregnancy tissue /products of conception (POCs) after miscarriage and is done to:

Identify chromosomal causes of miscarriage

Guide future pregnancy planning

Pediatric & Neonatal Testing

For infants and children and is recommended for:

Birth defects

Delayed growth or milestones

Abnormal NIPT results

Ambiguous genitalia

Cancer Cytogenetics

Karyotyping in canceer is recommended for:

Diagnosis of Leukemia

Treatment monitoring

Book a Karyotype Test

Sample Requirements for Karyotype Test

Depending on the test:

Blood sample (most common)

Tissue sample (POC or tumor)

Amniotic fluid (for prenatal test)

CVS (for prenatal test)

Turnaround Time

Standard karyotype: 7–14 days

Prenatal testing: 10–14 days

Why Choose our Lab?

High-resolution chromosomal analysis

Experienced molecular genetics team

Accurate and clinically validated results

Confidential and secure testing

Support for clinicians and patients

Frequently Asked Questions


Is karyotyping the same as DNA testing?

No. Karyotyping examines whole chromosomes, while DNA tests analyze specific genes.


Do I need a doctor’s referral?

Some tests (especially prenatal and cancer-related) may require a clinician’s request.


Can this test detect all genetic conditions?

No. It detects large chromosomal changes. Smaller mutations may require sequencing tests.


Do I need to prepare for the test?

No special preparation is usually required.


Is the test painful?

Only mild discomfort may be felt during sample collection, such as a blood draw.


Is karyotyping safe during pregnancy?

It is safe when done through appropriate procedures like amniocentesis or CVS under medical guidance.


Who should consider karyotyping?

People with infertility, repeated miscarriages, or suspected genetic conditions may benefit.


What is mosaicism?

It is a condition where some cells have different chromosome patterns, which karyotyping can sometimes detect.


What happens after I get my results?

A healthcare provider or genetic specialist will explain the results and next steps.


Can this test help with future pregnancy planning?

Yes, it can identify risks and help guide informed decisions.


What is the Cost of the Karyotype Test in Kenya?

Standard Karyotype (Blood) - 15,000 Kshs

Prenatal Karyotype (Amniotic fluid / CVS) - 15,000 Kshs

Miscarriage Analysis (POCs) - 40,000 Kshs

Couple Testing - 30,000 Kshs

Cancer Cytogenetics - Call to inquire


Book a Karyotype Test

15000

Completed DNA Tests

15000

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30000

Customer Services

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