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.

Also known asTranslocation T(9;22) Bcr-abl Philadelphia Chromosome By Karyotyping Bcr-abl Philadelphia Chromosome By Karyotyping

Available via

Home Collection, Lab Visit

Contains

5 parameters

Earliest reports in

10 Working Days

Test details

PHILADELPHIA CHROMOSOME Test in Vadodara Overview

Preparations

No special preparations needed

Test included
PHILADELPHIA CHROMOSOME includes 5 parameters

  • Specimen
  • Indications
  • Cells Counted & Analysed
  • Cells Karyotyped
  • Karyotype
Frequently Asked Questions

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
SpecimenVacutainerVolume
Bone MarrowOthers1 ML
Heparin Whole BloodGreen Vacutainer5 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

PHILADELPHIA CHROMOSOME

4900