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CLL FISH PANEL FISH del11q trisomy 12 del13q del17p Test Cost

Original price was: 3,960 د.إ.Current price is: 2,970 د.إ.

-25%

The CLL FISH Panel is a specialized diagnostic test performed to identify specific genetic abnormalities associated with Chronic Lymphocytic Leukemia (CLL), a type of cancer that affects the white blood cells. This test focuses on detecting the presence of four key genetic markers: deletion 11q (del11q), trisomy 12, deletion 13q (del13q), and deletion 17p (del17p), which have implications for prognosis and treatment strategies.

FISH, or Fluorescence In Situ Hybridization, is the technology used in this panel. It involves using fluorescent probes that bind to specific parts of chromosomes, making it possible to visualize genetic changes under a microscope. Each of the genetic abnormalities targeted by this panel has distinct prognostic significance. For example, del17p is associated with a more aggressive disease course and resistance to certain treatments, making its identification crucial for effective management of CLL.

The test is available at DNA Labs UAE, a leading facility in genetic diagnostics. The cost of the CLL FISH Panel test at DNA Labs UAE is 2970 AED. Given the detailed nature of this test, it provides essential information that can guide the choice of treatment, helping clinicians tailor therapy to the genetic profile of the leukemia, thus offering a more personalized approach to patient care.

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CLL FISH PANEL FISH del11q trisomy 12 del13q del17p Test

Test Name: CLL FISH PANEL FISH del11q trisomy 12 del13q del17p Test

Components: Sodium Heparin Vacutainer (2ml)

Price: 2970.0 AED

Sample Condition: Bone marrow / Peripheral blood (Transport immediately)

Report Delivery: 5-7 days

Method: FISH

Test type: Genetics

Doctor: Oncology

Test Department: Pre Test Information

CLL FISH PANEL (FISH del(11q), trisomy 12, del(13q), del(17p)]) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details

The CLL FISH panel is a diagnostic test used to detect specific genetic abnormalities in chronic lymphocytic leukemia (CLL) patients. The panel specifically looks for four genetic abnormalities: del(11q), trisomy 12, del(13q), and del(17p).

  1. del(11q): This refers to the deletion of a specific portion of chromosome 11. It is associated with a poor prognosis in CLL patients, as it is often linked to more aggressive disease and resistance to treatment.
  2. Trisomy 12: Trisomy refers to the presence of an extra copy of a chromosome. In CLL, trisomy 12 refers to the presence of an extra copy of chromosome 12. This abnormality is associated with a more indolent (slow-growing) form of CLL.
  3. del(13q): Similar to del(11q), this refers to the deletion of a specific portion of chromosome 13. It is the most common genetic abnormality in CLL and is generally associated with a good prognosis.
  4. del(17p): This refers to the deletion of a specific portion of chromosome 17. It is associated with a very poor prognosis in CLL patients, as it is often linked to treatment resistance and shorter overall survival.

The CLL FISH panel uses fluorescence in situ hybridization (FISH) technique to detect these specific genetic abnormalities. It helps in providing important prognostic information and guiding treatment decisions for CLL patients.

Test Name CLL FISH PANEL FISH del11q trisomy 12 del13q del17p Test
Components Sodium Heparin Vacutainer (2ml)
Price 2970.0 AED
Sample Condition Bone marrow \/ Peripheral blood (Transport immediately)
Report Delivery 5-7 days
Method FISH
Test type Genetics
Doctor Oncology
Test Department:
Pre Test Information CLL FISH PANEL (FISH del(11q), trisomy 12, del(13q), del(17p)]) 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 FISH panel is a diagnostic test used to detect specific genetic abnormalities in chronic lymphocytic leukemia (CLL) patients. The panel specifically looks for four genetic abnormalities: del(11q), trisomy 12, del(13q), and del(17p).

1. del(11q): This refers to the deletion of a specific portion of chromosome 11. It is associated with a poor prognosis in CLL patients, as it is often linked to more aggressive disease and resistance to treatment.

2. Trisomy 12: Trisomy refers to the presence of an extra copy of a chromosome. In CLL, trisomy 12 refers to the presence of an extra copy of chromosome 12. This abnormality is associated with a more indolent (slow-growing) form of CLL.

3. del(13q): Similar to del(11q), this refers to the deletion of a specific portion of chromosome 13. It is the most common genetic abnormality in CLL and is generally associated with a good prognosis.

4. del(17p): This refers to the deletion of a specific portion of chromosome 17. It is associated with a very poor prognosis in CLL patients, as it is often linked to treatment resistance and shorter overall survival.

The CLL FISH panel uses fluorescence in situ hybridization (FISH) technique to detect these specific genetic abnormalities. It helps in providing important prognostic information and guiding treatment decisions for CLL patients.

SKU: TEST-4717 Category:

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