Cystic Fibrosis Mutation Detection Test
The Cystic Fibrosis Mutation Detection Test is a vital diagnostic tool used to identify mutations in the CFTR gene, which are responsible for cystic fibrosis (CF), a genetic disorder that affects the lungs, pancreas, and other organs. This test is essential for early diagnosis, enabling timely intervention and management of the disease, which can significantly improve the quality of life for patients.
What the Test Measures
This test specifically detects mutations in the CFTR gene. By analyzing the genetic material, healthcare providers can determine whether an individual carries one or more mutations associated with cystic fibrosis. This is crucial for individuals exhibiting symptoms or those with a family history of the disease.
Who Should Consider This Test
- Individuals with a family history of cystic fibrosis.
- Newborns showing symptoms such as persistent cough, difficulty in breathing, or poor weight gain.
- Patients with unexplained respiratory issues or pancreatic insufficiency.
Benefits of Taking the Test
Taking the Cystic Fibrosis Mutation Detection Test offers several benefits:
- Early detection of cystic fibrosis allows for prompt treatment and management strategies.
- Informs family planning decisions for those with a known family history.
- Helps in understanding the prognosis and potential complications associated with the disease.
Understanding Your Results
Results from the Cystic Fibrosis Mutation Detection Test will indicate whether mutations are present in the CFTR gene. A positive result means that the individual has one or more mutations associated with cystic fibrosis, while a negative result indicates the absence of these mutations. It is important to discuss your results with a healthcare provider to understand their implications fully.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Cystic Fibrosis Mutation Detection Test | 24,000 KSh | 36,000 KSh |
Sample Requirements
For this test, a sample of 4 mL (2 mL min.) of whole blood in a lavender top (EDTA) tube or 10 mL of amniotic fluid in a sterile screw-capped container is required. It is crucial to ship the sample refrigerated and not to freeze it. Additionally, a duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for processing.
Branches and Booking
We have branches across all major cities in Kenya, making it convenient for you to access our services. We also offer home sample collection for your convenience.
Book the Cystic Fibrosis Mutation Detection Test today! For more information, call or WhatsApp us at +254711564616.
