Acute Lymphoblastic Leukemia All Cytogenetics Panel Test
Introduction
The Acute Lymphoblastic Leukemia All Cytogenetics Panel Test is a critical diagnostic tool for identifying genetic abnormalities associated with acute lymphoblastic leukemia (ALL). This test plays a pivotal role in determining the most effective treatment strategies for patients diagnosed with this type of cancer. By analyzing specific chromosomal changes, healthcare providers can gain insights into the prognosis and potential response to therapy.
What the Test Measures
This comprehensive panel assesses various genetic components, including:
- BCR/ABL or Philadelphia translocation
- t(variable;11q23) – MLL gene breakapart
- t(12;21)(p13;q22) – TEL/AML1
- Chromosome analysis for hematological malignancies
Who Should Consider This Test?
Patients exhibiting symptoms of acute lymphoblastic leukemia or those at high risk due to family history or previous medical conditions should consider this test. Symptoms may include:
- Unexplained fatigue
- Frequent infections
- Easy bruising or bleeding
- Pale skin
Benefits of Taking the Test
The benefits of the Acute Lymphoblastic Leukemia All Cytogenetics Panel Test include:
- Accurate diagnosis of ALL
- Informed treatment planning based on genetic findings
- Monitoring of treatment effectiveness and disease progression
Understanding Your Results
Results from the test will provide valuable information regarding the presence of specific genetic abnormalities. A hematologist will interpret these results and discuss their implications for treatment and prognosis. It is essential to follow up with your healthcare provider for a comprehensive understanding of your results.
Test Name and Price
| Discount Price | 400000 NGN |
|---|---|
| Regular Price | 540000 NGN |
Book Your Test Today!
To schedule your Acute Lymphoblastic Leukemia All Cytogenetics Panel Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have.
Pre-Test Instructions
It is mandatory to bring a duly filled Chromosome and FISH analysis Requisition form (Form 17) when coming for the test. The sample type required includes:
- 8 mL (6 mL min.) whole blood from 2 Green Top (Sodium Heparin) tubes
- 4 mL (2 mL min.) Bone Marrow from 1 Green Top (Sodium Heparin) tube
Please ensure that samples are shipped at 18-22°C and do not freeze.
Turnaround Time
Samples are accepted daily by 4 PM, and reports will be ready within 4 working days.
