Chronic Lymphocytic Leukemia CLL Mutations Detection Panel 2 Test
Introduction
The Chronic Lymphocytic Leukemia CLL Mutations Detection Panel 2 Test is an advanced diagnostic tool used to detect specific genetic mutations in patients diagnosed with chronic lymphocytic leukemia (CLL). This test is vital for oncologists as it provides insights into the genetic landscape of the disease, allowing for personalized treatment strategies that can significantly improve patient outcomes.
What the Test Measures
This panel tests for several key mutations associated with CLL, including:
- SF3B1 K700E mutation
- MYD88 L265P mutation
- NOTCH1 p.2514 fs mutation
- PTEN loss at 10q23.31
- 11q deletion
- Trisomy 12
- 13q14 deletion
- 14q deletion
- 17p deletion
- Trisomy 19
Who Should Consider This Test
This test is recommended for patients diagnosed with CLL or those exhibiting symptoms such as:
- Persistent fatigue
- Unexplained weight loss
- Swollen lymph nodes
- Frequent infections
Individuals with a family history of CLL or other hematological malignancies may also benefit from this test.
Benefits of Taking the Test
Taking the Chronic Lymphocytic Leukemia CLL Mutations Detection Panel 2 Test offers several benefits:
- Helps oncologists determine the most effective treatment options.
- Provides insights into the prognosis of the disease.
- Facilitates early intervention strategies.
- Enhances understanding of disease progression.
Understanding Your Results
Once the results are available, your oncologist will discuss the findings with you. It is essential to understand that the presence of certain mutations may indicate a more aggressive form of CLL, which could necessitate more intensive treatment. Conversely, the absence of these mutations may suggest a more favorable prognosis.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 100,000 NGN | 150,000 NGN |
Booking the Test
To book the Chronic Lymphocytic Leukemia CLL Mutations Detection Panel 2 Test, please contact us at +2348077798758. Ensure to fill out the Genomics Clinical Information Requisition Form (Form 20) before your visit. The sample required is 4 mL (2 mL min.) of whole blood from a lavender top (EDTA) tube, shipped refrigerated. Please do not freeze the sample.
Turnaround time for results is typically one week, with samples collected by 11 am on Mondays and reports available by Saturday.
