
IGHV Gene Mutation Analysis near me in Agra







The immunoglobulin heavy chain variable region gene (IgHV) mutation status has been an established prognostic factor in patients with CLL. B-cells harboring IGHV help fight infections by making antibodies. In a disease called Chronic Lymphocytic Leukemia (CLL), some B-cells become unhealthy and grow out of control. Doctors look at the changes in the IGHV to understand how the CLL might behave.
This is a PCR-based investigational test to determine the mutational status of IGHV by employing multiple consensus DNA primers that target conserved genetic regions within the immunoglobulin heavy chain (IGH) gene.
The IGHV mutation status acts as a crucial prognostic indicator, distinguishing between mutated (M-CLL) and unmutated (UM-CLL) subtypes, guiding treatment approaches, and predicting response to therapy, ultimately shaping personalized management strategies for patients.











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- CBC (Complete Blood Count)
- FBS (Fasting Blood Sugar)
- Thyroid Profile Total (T3, T4 & TSH)
- HbA1c (Glycosylated Hemoglobin)
- PPBS (Postprandial Blood Sugar)
- Lipid Profile
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- LFT (Liver Function Test)
- KFT (Kidney Function Test)
- TSH (Thyroid Stimulating Hormone) Ultrasensitive
- ESR (Erythrocyte Sedimentation Rate)
- Uric Acid, Serum
- Vitamin B12
- CRP (C-Reactive Protein), Quantitative
- Urine C/S (Urine Culture and Sensitivity)
- Serum Electrolytes
- Serum Calcium
- Serum Creatinine
- Diabetes Screening (HbA1C & Fasting Sugar)
- KFT with Electrolytes (Kidney Function Test with Electrolytes)
- Cholesterol - Total
- Hb (Hemoglobin)
- Complete Hemogram (CBC & ESR)















