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Chronic Lymphocytic Leukemia CLL Mutations Detection Panel 1 Test

820 د.إ

-10%

The “Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test” is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify specific genetic mutations associated with CLL. This test plays a crucial role in the precise diagnosis and management of CLL, a type of cancer characterized by the accumulation of abnormal lymphocytes in the blood and bone marrow. By analyzing the patient’s DNA, the test can detect mutations that are known to influence the disease’s behavior, prognosis, and response to treatment. The cost of the test is 820 AED, making it a valuable tool for healthcare professionals in tailoring personalized treatment plans for CLL patients, enhancing the effectiveness of therapy, and potentially improving patient outcomes.

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CHRONIC LYMPHOCYTIC LEUKEMIA CLL MUTATIONS DETECTION PANEL 1 Test

Are you concerned about Chronic Lymphocytic Leukemia (CLL)? DNA Labs UAE offers the CLL Mutations Detection Panel 1 Test to help diagnose and understand this type of cancer.

Test Details

The Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test is a diagnostic test used to identify specific genetic mutations associated with CLL, a type of cancer that affects the white blood cells called lymphocytes. This test analyzes the DNA or RNA of the patient’s blood or bone marrow sample to detect mutations in genes such as TP53, NOTCH1, SF3B1, and ATM, among others. By identifying these mutations, healthcare professionals can better understand the prognosis of the patient, determine the most appropriate treatment options, and monitor the progression of the disease. The CLL Mutations Detection Panel 1 Test is typically performed alongside other tests, such as flow cytometry and cytogenetic analysis, to provide a comprehensive evaluation of the patient’s condition.

Test Components

  • Chromosome 2p gain
  • 6q deletion
  • 8p loss & 8q amplification
  • 9p21 loss
  • 11q deletion
  • Trisomy 12
  • 13q14 deletion
  • 17p deletion

Test Cost

The cost of the CLL Mutations Detection Panel 1 Test is AED 820.0.

Sample Condition

For this test, a 4 mL (2 mL min.) whole blood sample is required from 1 Lavender top (EDTA) tube. The sample should be shipped refrigerated and must not be frozen. Additionally, a duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Report Delivery

The sample should be submitted by Monday at 11 am, and the report will be delivered on Saturday.

Method

The CLL Mutations Detection Panel 1 Test is performed using PCR – MLPA method.

Test Type

This test falls under the category of cancer tests.

Doctor

The test is recommended to be conducted by an Oncologist.

Test Department

The CLL Mutations Detection Panel 1 Test is conducted in the Molecular Diagnostics department.

Pre Test Information

A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory before conducting the test.

Don’t let CLL take control of your life. Visit DNA Labs UAE and get the CLL Mutations Detection Panel 1 Test done today to gain valuable insights into your condition and determine the best course of action for your treatment.

Test Name CHRONIC LYMPHOCYTIC LEUKEMIA CLL MUTATIONS DETECTION PANEL 1 Test
Components *Chromosome 2p gain*6q deletion*8p loss & 8q amplification*9p21 loss*11q deletion *Trisomy 12*13q14 deletion*17p deletion
Price 820.0 AED
Sample Condition 4 mL (2 mL min.) whole blood from 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery SampleMon by 11 am;ReportSat
Method PCR – MLPA
Test type Cancer
Doctor Oncologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

The Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test is a diagnostic test used to identify specific genetic mutations associated with CLL, a type of cancer that affects the white blood cells called lymphocytes. This test analyzes the DNA or RNA of the patient’s blood or bone marrow sample to detect mutations in genes such as TP53, NOTCH1, SF3B1, and ATM, among others.

By identifying these mutations, healthcare professionals can better understand the prognosis of the patient, determine the most appropriate treatment options, and monitor the progression of the disease. The CLL Mutations Detection Panel 1 Test is typically performed alongside other tests, such as flow cytometry and cytogenetic analysis, to provide a comprehensive evaluation of the patient’s condition.