Cystic Fibrosis DNA Test

Cystic Fibrosis is an autosomal recessive monogenic condition caused by pathogenic variants in the CFTR gene, leading to thick mucus accumulation in the lungs, digestive system, and other organs.

Indications: Why test CFTR?

Clinical symptoms of CF (chronic pulmonary infections, pancreatic insufficiency).
Carrier screening for prospective parents with a family history of CF.
Infertility evaluation (e.g., congenital bilateral absence of the vas deferens in males).

When should I take the test? Ideal for pre-conception planning or clinical diagnosis of suggestive respiratory/digestive symptoms.

Do I need to fast or prepare? No special preparation or fasting is required.

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Test Summary Specs

Turnaround Time	7 to 10 Business Days
Estimated Cost	KES 28,000 – KES 38,000
Methodology	Targeted PCR / Sanger / NGS Variant Panel
Sample Type	5 mL Peripheral Whole Blood (EDTA), Buccal Swabs, or Prenatal Samples
Clinical Use	Diagnostic Confirmation, Carrier Screening, Reproductive Risk Assessment