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CLL NGS Panel FISH and KT and IGVH Mutation Analysis and NGS TP53 Mutation Analysis Test

9,360 د.إ

-10%

The CLL NGS Panel FISH, KT, IGVH Mutation Analysis, and NGS TP53 Mutation Analysis Test is a comprehensive diagnostic examination offered by DNA Labs UAE, designed specifically for patients suspected of having Chronic Lymphocytic Leukemia (CLL). This test employs advanced Next-Generation Sequencing (NGS) technology, Fluorescence In Situ Hybridization (FISH) techniques, Karyotyping (KT), and IGVH mutation analysis to provide a detailed genetic profile of the CLL. Additionally, it includes an NGS-based TP53 mutation analysis, which is crucial for understanding the disease’s prognosis and guiding treatment decisions.

The test aims to identify genetic mutations and chromosomal abnormalities that are characteristic of CLL, which can help in confirming the diagnosis, predicting disease progression, and selecting the most effective treatment options. The IGVH mutation status is particularly important, as it can significantly influence the patient’s response to certain therapies. Similarly, the TP53 mutation status is a key prognostic marker, with mutations in this gene often associated with a more aggressive disease course and resistance to standard treatments.

The cost of this comprehensive test is 9360 AED, reflecting the extensive insights it provides into the genetic landscape of CLL. By opting for this test at DNA Labs UAE, patients and healthcare providers can access crucial information that will aid in the tailored management of Chronic Lymphocytic Leukemia, potentially leading to better outcomes.

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CLL NGS PANEL FISH and KT and IGVH Mutation Analysis and NGS TP53 Mutation Analysis Test

Test Name: CLL NGS PANEL FISH and KT and IGVH Mutation Analysis and NGS TP53 Mutation Analysis

Components: Sodium Heparin Vacutainer (2ml) + EDTA Vacutainer (2ml)

Price: 9360.0 AED

Sample Condition: Peripheral blood + FFPE BLOCK

Report Delivery: 15-18 days

Method: Cell Culture + FISH + PCR + NGS

Test Type: Genetics

Doctor: Gynecologist

Test Department: Pre Test Information

CLL NGS PANEL (FISH + KT + IGVH Mutation Analysis + NGS TP53 Mutation Analysis) can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details:

The CLL NGS panel is a comprehensive genetic testing panel that combines several different tests to provide a comprehensive analysis of chronic lymphocytic leukemia (CLL). The panel includes fluorescence in situ hybridization (FISH), karyotyping (KT), IGVH mutation analysis, and NGS TP53 mutation analysis.

FISH is a technique used to detect specific genetic abnormalities in CLL cells. This test is useful for identifying common chromosomal abnormalities associated with CLL, such as deletion of chromosome 13q, deletion of chromosome 11q, and trisomy 12.

KT is a test that examines the structure and number of chromosomes in CLL cells. This test can identify large-scale chromosomal abnormalities, such as translocations or deletions, that may be missed by FISH.

IGVH mutation analysis is a test that examines the mutations in the immunoglobulin variable region genes. This test is important for predicting the course of the disease and response to treatment.

NGS TP53 mutation analysis is a test that examines mutations in the TP53 gene, which is commonly mutated in CLL. This test is important for predicting treatment response and overall prognosis.

By combining these tests, the CLL NGS panel provides a comprehensive analysis of CLL genetics, which can help guide treatment decisions and improve patient outcomes.

Test Name CLL NGS PANEL FISH andKT and IGVH Mutattion Analysisand NGS TP53 mutation analysis Test
Components Sodium Heparin Vacutainer (2ml)+ EDTA Vacutainer (2ml)
Price 9360.0 AED
Sample Condition Peripheral blood + FFPE BLOCK
Report Delivery 15-18 days
Method Cell Culture + FISH+PCR+NGS
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information CLL NGS PANEL (FISH +KT + IGVH Mutattion Analysis+ NGS TP53 mutation analysis) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

The CLL NGS panel is a comprehensive genetic testing panel that combines several different tests to provide a comprehensive analysis of chronic lymphocytic leukemia (CLL). The panel includes fluorescence in situ hybridization (FISH), karyotyping (KT), IGVH mutation analysis, and NGS TP53 mutation analysis.

FISH is a technique used to detect specific genetic abnormalities in CLL cells. This test is useful for identifying common chromosomal abnormalities associated with CLL, such as deletion of chromosome 13q, deletion of chromosome 11q, and trisomy 12.

KT is a test that examines the structure and number of chromosomes in CLL cells. This test can identify large-scale chromosomal abnormalities, such as translocations or deletions, that may be missed by FISH.

IGVH mutation analysis is a test that examines the mutations in the immunoglobulin variable region genes. This test is important for predicting the course of the disease and response to treatment.

NGS TP53 mutation analysis is a test that examines mutations in the TP53 gene, which is commonly mutated in CLL. This test is important for predicting treatment response and overall prognosis.

By combining these tests, the CLL NGS panel provides a comprehensive analysis of CLL genetics, which can help guide treatment decisions and improve patient outcomes.

SKU: TEST-705 Category:

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