Philadelphia Chromosome
A test to detect the Philadelphia chromosome by karyotyping, which involves visualizing chromosomal abnormalities under a microscope. This test is used to confirm the presence of the BCR-ABL fusion gene associated with CML. It is important for diagnosis and assessing prognosis.
Philadelphia Chromosome Test in Narendrapur Overview
No special preparations needed
- Specimen
- Indications
- Cells Counted & Analysed
- Cells Karyotyped
- Karyotype
This test detects the presence of the Philadelphia chromosome, a genetic abnormality linked to chronic myeloid leukemia (CML) and some acute leukemias.
Patients with suspected leukemia or abnormal blood cell counts may be advised to take this test.
A blood or bone marrow sample is analyzed using genetic techniques like fluorescence in situ hybridization (FISH) or polymerase chain reaction (PCR).
A positive result confirms the presence of the Philadelphia chromosome, guiding treatment options such as targeted therapies like tyrosine kinase inhibitors (TKIs).
Yes, targeted therapies have significantly improved survival rates for Philadelphia chromosome-positive leukemia patients.
Test code
5834
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Bone Marrow | Others | 1 ML |
| Heparin Whole Blood | Green Vacutainer | 5 ML |
Specimen stability information
Bone Marrow, Heparin Whole Blood
Collection instructions
Age,Gender,Clinical history required
Specimen rejection criteria
Test run frequency
Monday,Tuesday,Wednesday,Thursday,Friday TIME - 07:00
Turn around time
10 Working Days
Performing locations
Department
- Cytogenetics
CPT and Loinc codes
Package price
₹4900
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₹4900