IGVH Gene Mutation Detection Test, Price, Normal Range | Sprint Diagnostics Hyderabad

Patient Preparing : No fasting or specific preparation is required for this test. Regular consumption of water and prescribed medication (unless advised otherwise by your physician) can continue.

₹ 13000


The IGHV gene mutation detection is a highly specialized test that is often recommended in the management of certain types of blood cancers, specifically chronic lymphocytic leukemia (CLL) and some types of non-Hodgkin lymphoma (NHL). The test analyzes the status of mutations in the Immunoglobulin Heavy Chain Variable Region (IGHV) gene, which provides valuable prognostic information for these diseases. This test helps physicians to tailor treatments and predict the likely course of the disease more accurately.

Mutations in the IGHV gene are a natural process that occurs in healthy B-cells (a type of white blood cell) during the immune response. However, when these mutated B-cells become cancerous, their IGHV mutation status can have a significant impact on the course of the disease. CLL or NHL patients whose cancers have unmutated IGHV genes generally have a more aggressive disease and a poorer prognosis compared to those with mutated IGHV genes.

Test Name IGVH Gene Mutation Detection
Sample Type Blood
Preparations Required No fasting or specific preparation is required for this test. Regular consumption of water and prescribed medication (unless advised otherwise by your physician) can continue.
Report Time 18 days
Price in Hyderabad ₹ 13000

Why is the IGHV gene mutation detection test performed?

The IGHV gene mutation detection test is primarily performed to help predict the disease course in patients with CLL or certain types of NHL. It guides doctors in formulating a suitable treatment strategy based on the mutation status.

How is the test performed?

The test requires a sample of your blood or bone marrow, which is then sent to the laboratory for detailed genetic analysis.

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What do the results mean?

If your IGHV genes are mutated, it generally indicates a more indolent disease course with a better prognosis. If your IGHV genes are unmutated, it suggests a more aggressive disease with a poorer prognosis.

How often should this test be performed?

The IGHV mutation test is typically performed at diagnosis to establish the prognosis. Repeat testing is usually not required unless there's a transformation of the disease or if the first test was inconclusive.

Are there any precautions to be taken before the test?

There are no specific precautions for this test. You should continue your regular diet, water intake, and medication (unless advised otherwise by your physician).

What factors can affect the results of the test?

The accuracy of the test results can be affected by certain technical factors such as the quality of the sample collected or errors during the processing in the lab.

What are the normal values for this test?

In the context of this test, "normal" isn't a relevant term. It's about whether the IGHV genes are mutated or unmutated, and each condition has a different prognostic implication.

Who should I consult if my test results are abnormal?

If your test results indicate an unmutated IGHV status (which is associated with a more aggressive disease course), you should consult with a hematologist or oncologist experienced in managing CLL or NHL.

Is there any preparation required before the test?

No special preparation is needed for this test. You should continue with your normal routine and medications unless otherwise instructed by your doctor.

Are there any lifestyle modifications that can affect the IGHV gene mutation status?

No, the IGHV gene mutation status is a genetic characteristic of the cancer cells and is not influenced by lifestyle factors.

Can the test be performed at home?

No, the IGHV gene mutation detection test requires a blood or bone marrow sample to be taken, which should be done in a clinical setting by a healthcare professional.

How is this test different from other genetic tests?

The IGHV gene mutation test is specifically designed to analyze the mutation status of the IGHV genes in B-cells, which provides prognostic information in CLL and certain types of NHL.

Can the IGHV gene mutation status change over time?

Generally, the IGHV gene mutation status does not change over time in CLL or NHL, although rare exceptions may exist.

Does a "mutated" or "unmutated" result mean that I have a genetic disorder that I can pass on to my children?

No, the IGHV mutation status is not a heritable trait. It is a characteristic of the cancer cells and does not affect your genetic makeup or that of your offspring.

What other tests might be performed along with the IGHV gene mutation detection test?

Other tests that might be performed include flow cytometry, FISH analysis (fluorescence in situ hybridization), and cytogenetics to gain a comprehensive understanding of the disease.

This understanding of the IGHV gene mutation detection test's importance can provide patients with a clearer perspective on their disease and how to manage it best. This test offers valuable insights into the likely course of the disease and assists physicians in developing the most appropriate treatment strategies. If you have any further questions, always consult with your healthcare provider to get the best medical advice.

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