Depending on the test:
Blood sample (most common)
Tissue sample (POC or tumor)
Amniotic fluid (for prenatal test)
CVS (for prenatal test)
Standard karyotype: 7–14 days
Prenatal testing: 10–14 days
High-resolution chromosomal analysis
Experienced molecular genetics team
Accurate and clinically validated results
Confidential and secure testing
Support for clinicians and patients
No. Karyotyping examines whole chromosomes, while DNA tests analyze specific genes.
Some tests (especially prenatal and cancer-related) may require a clinician’s request.
No. It detects large chromosomal changes. Smaller mutations may require sequencing tests.
No special preparation is usually required.
Only mild discomfort may be felt during sample collection, such as a blood draw.
It is safe when done through appropriate procedures like amniocentesis or CVS under medical guidance.
People with infertility, repeated miscarriages, or suspected genetic conditions may benefit.
It is a condition where some cells have different chromosome patterns, which karyotyping can sometimes detect.
A healthcare provider or genetic specialist will explain the results and next steps.
Yes, it can identify risks and help guide informed decisions.
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
15000
15000
30000
99.9
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