CLL Panel Cytogenetics and FISH del11q Trisomy 12 del13q del17p Test sale cost 3600 AED
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CLL Panel Cytogenetics and FISH del11q Trisomy 12 del13q del17p Test Cost

Original price was: 4,800 د.إ.Current price is: 3,600 د.إ.

-25%

The “CLL Panel Cytogenetics and FISH del11q Trisomy 12 del13q del17p Test” is a specialized diagnostic procedure aimed at patients with Chronic Lymphocytic Leukemia (CLL), one of the most common types of leukemia in adults. This comprehensive test combines cytogenetic analysis and Fluorescence In Situ Hybridization (FISH) to detect specific genetic abnormalities associated with CLL, namely deletions in chromosomes 11q, 13q, 17p, and trisomy of chromosome 12.

Cytogenetics involves examining the chromosomes in cells to identify structural changes that may lead to disease, while FISH is a more targeted approach that uses fluorescent probes to visualize specific DNA sequences on chromosomes. Together, these methodologies offer a powerful tool for the precise identification of genetic markers critical for prognosis and treatment planning in CLL patients.

The test, which costs 3600 AED, is conducted at DNA Labs UAE, a facility known for its advanced diagnostic capabilities and expertise in genetic testing. The results from this panel are pivotal for clinicians in tailoring treatment strategies, predicting disease progression, and ultimately improving patient outcomes.

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CLL PANEL Cytogenetics and FISH del11q trisomy 12 del13q del17p Test

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

Components: Sodium Heparin Vacutainer (2ml)

Price: 3600.0 AED

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

Report Delivery: 5-7 days

Method: Cell Culture + FISH

Test Type: Genetics

Doctor: Gynecologist

Test Department: Pre Test Information

CLL PANEL (Cytogenetics + FISH del(11q), trisomy 12, del(13q), del(17p)]) 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 panel is a diagnostic test used to detect specific genetic abnormalities in patients with chronic lymphocytic leukemia (CLL). It combines cytogenetic analysis and fluorescence in situ hybridization (FISH) to identify four common genetic abnormalities associated with CLL:

  1. del(11q): This refers to the deletion of a portion of chromosome 11. It is associated with a more aggressive form of CLL and is often associated with a poor prognosis.
  2. trisomy 12: Trisomy 12 refers to the presence of an extra copy of chromosome 12. It is one of the most common genetic abnormalities in CLL and is associated with a more indolent (slow-growing) form of the disease.
  3. del(13q): This refers to the deletion of a portion of chromosome 13. It is the most common genetic abnormality in CLL and is generally associated with a more favorable prognosis.
  4. del(17p): This refers to the deletion of a portion of chromosome 17, specifically the region containing the TP53 gene. This genetic abnormality is associated with a very poor prognosis and resistance to certain treatments.

The CLL panel is performed on a sample of the patient’s blood or bone marrow. Cytogenetic analysis involves examining the chromosomes under a microscope to detect large-scale abnormalities such as deletions or trisomies. FISH is a molecular technique that uses fluorescently labeled probes to specifically target and detect the presence or absence of specific genetic abnormalities.

By identifying these genetic abnormalities, the CLL panel can help guide treatment decisions and provide prognostic information for patients with CLL.

Test Name CLL PANEL Cytogenetics and FISH del11q trisomy 12 del13q del17p Test
Components Sodium Heparin Vacutainer (2ml)
Price 3600.0 AED
Sample Condition Bone marrow \/ Peripheral blood (Transport immediately)
Report Delivery 5-7 days
Method Cell Culture + FISH
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information CLL PANEL (Cytogenetics + 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 panel is a diagnostic test used to detect specific genetic abnormalities in patients with chronic lymphocytic leukemia (CLL). It combines cytogenetic analysis and fluorescence in situ hybridization (FISH) to identify four common genetic abnormalities associated with CLL.

1. del(11q): This refers to the deletion of a portion of chromosome 11. It is associated with a more aggressive form of CLL and is often associated with a poor prognosis.

2. trisomy 12: Trisomy 12 refers to the presence of an extra copy of chromosome 12. It is one of the most common genetic abnormalities in CLL and is associated with a more indolent (slow-growing) form of the disease.

3. del(13q): This refers to the deletion of a portion of chromosome 13. It is the most common genetic abnormality in CLL and is generally associated with a more favorable prognosis.

4. del(17p): This refers to the deletion of a portion of chromosome 17, specifically the region containing the TP53 gene. This genetic abnormality is associated with a very poor prognosis and resistance to certain treatments.

The CLL panel is performed on a sample of the patient’s blood or bone marrow. Cytogenetic analysis involves examining the chromosomes under a microscope to detect large-scale abnormalities such as deletions or trisomies. FISH is a molecular technique that uses fluorescently labeled probes to specifically target and detect the presence or absence of specific genetic abnormalities.

By identifying these genetic abnormalities, the CLL panel can help guide treatment decisions and provide prognostic information for patients with CLL.

SKU: TEST-4646 Category:

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