Sale!

WT-1 Mutation Detection Test Cost

Original price was: 2,400 د.إ.Current price is: 2,040 د.إ.

-15%

The WT-1 Mutation Detection Test is a specialized genetic test designed to identify mutations in the WT1 gene, which plays a crucial role in kidney development and function. Abnormalities in this gene are associated with a range of health issues, most notably Wilms tumor, a type of kidney cancer primarily affecting children, as well as certain syndromes and kidney-related disorders. This test is critical for early diagnosis and guiding treatment strategies, including surgical interventions, chemotherapy, and targeted therapies.

Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services, the test offers a comprehensive analysis of the WT1 gene to detect mutations that could indicate a predisposition to Wilms tumor and other related conditions. The cost of the WT-1 Mutation Detection Test is 2040 AED, reflecting the sophisticated technology and expertise required to accurately identify and interpret genetic variations in the WT1 gene. This investment can be invaluable for affected families, providing essential information for managing and potentially mitigating the impact of associated health issues.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

WT-1 MUTATION DETECTION Test

At DNA Labs UAE, we offer the WT-1 mutation detection test, a medical test used to detect mutations in the WT-1 gene. This gene is responsible for encoding a protein that plays a crucial role in normal kidney development and function.

Price: 2040.0 AED

Sample Condition: 4 mL (2 mL min.) whole blood / Bone marrow in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.

Report Delivery: Sample Daily by 11 am; Report 18 days

Method: PCR Sequencing

Test Type: Cancer

Doctor: Nephrologist

Test Department: MOLECULAR DIAGNOSTICS

Pre Test Information: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Test Details:

The WT-1 mutation detection test is used to identify mutations in the WT-1 gene. Mutations in this gene have been associated with various conditions, including Wilms tumor (a type of kidney cancer) and certain cases of kidney failure.

The test involves collecting a sample of blood, tissue, or other bodily fluids from the patient. This sample is then analyzed in our laboratory using techniques such as DNA sequencing or polymerase chain reaction (PCR) to identify any mutations or abnormalities in the WT-1 gene.

The results of this test can provide valuable insights into the underlying cause of a patient’s symptoms or conditions related to kidney function. This information can guide treatment decisions and prognosis.

It is important to note that the WT-1 mutation detection test should be ordered by a healthcare provider and interpreted by a qualified medical professional. Genetic testing can have significant implications, and genetic counseling is often recommended before and after undergoing such testing.

Test Name WT-1 MUTATION DETECTION Test
Components
Price 2040.0 AED
Sample Condition 4 mL (2 mL min.) whole blood \/ Bone marrow in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery Sample Daily by 11 am; Report 18 days
Method PCR Sequencing
Test type Cancer
Doctor Nephrologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Dulyfilled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

The WT-1 mutation detection test is a medical test used to detect mutations in the WT-1 gene. The WT-1 gene is responsible for encoding a protein that plays a crucial role in normal kidney development and function. Mutations in this gene have been associated with a variety of conditions, including Wilms tumor (a type of kidney cancer) and certain cases of kidney failure.

The test typically involves collecting a sample of blood, tissue, or other bodily fluids from the patient. This sample is then analyzed in a laboratory to look for any mutations or abnormalities in the WT-1 gene. Various techniques, such as DNA sequencing or polymerase chain reaction (PCR), may be used to identify these mutations.

The results of the WT-1 mutation detection test can help healthcare providers determine the underlying cause of a patient’s symptoms or conditions related to kidney function. This information can be used to guide treatment decisions and provide valuable insights into the patient’s prognosis.

It is important to note that the WT-1 mutation detection test is typically ordered by a healthcare provider and should be interpreted by a qualified medical professional. Genetic testing can have significant implications for patients and their families, and genetic counseling is often recommended before and after undergoing such testing.