WT1 Mutation Detection Test
Introduction
The WT1 Mutation Detection Test is a specialized diagnostic tool designed to identify mutations in the WT1 gene, which plays a critical role in cell growth and development. Mutations in this gene are often associated with various cancers, making this test vital for early detection and treatment planning. With advancements in molecular diagnostics, the WT1 test offers a reliable method for assessing genetic risks in patients.
What the Test Measures
This test detects specific mutations in the WT1 gene, which can indicate the presence of certain cancers. By analyzing a sample of whole blood or bone marrow, healthcare providers can gain insights into the genetic factors contributing to a patient’s condition.
Who Should Consider This Test
Individuals who may benefit from the WT1 Mutation Detection Test include:
- Patients exhibiting symptoms of cancer.
- Individuals with a family history of cancers associated with WT1 mutations.
- Patients undergoing treatment for cancer who need to assess their genetic status.
Benefits of Taking the Test
The WT1 Mutation Detection Test offers several benefits:
- Early detection of potential cancers, leading to timely interventions.
- Informed treatment decisions based on genetic insights.
- Personalized healthcare strategies tailored to the patient’s genetic makeup.
Understanding Your Results
Results from the WT1 Mutation Detection Test provide crucial information about the presence of WT1 mutations. Your healthcare provider will guide you through the interpretation of your results, helping you understand their implications for your health and treatment options.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 240,000 NGN |
| Regular Price | 360,000 NGN |
How to Book the Test
To book the WT1 Mutation Detection Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your test and answering any questions you may have.
Additional Information
Turnaround Time: Sample must be received daily by 11 AM; report available in 18 days.
Sample Type: 4 mL (2 mL min.) whole blood or bone marrow in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
Pre-Test Instructions: A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Specialty: Nephrologist
Department: Molecular Diagnostics
Method: PCR Sequencing
Disease Type: Cancer
