ACUTE MYELOID LEUKEMIA (AML)

This test assesses genetic mutations in AML patients with normal cytogenetics. It focuses on FLT3, NPM1, and CEBPA mutations that can impact disease prognosis. The results guide therapeutic choices for patients without major chromosomal abnormalities.

Also known asAml With Normal Cytogenetics (flt3Npm1Cebpa) Aml With Normal Cytogenetics (flt3Npm1

Available via

Home Collection, Lab Visit

Contains

13 parameters

Earliest reports in

7 Working Days

Test details

ACUTE MYELOID LEUKEMIA (AML) Package in Vadodara Overview

Preparations

No special preparations needed

Test included
ACUTE MYELOID LEUKEMIA (AML) includes 13 parameters

  • Specimen Source
  • Preliminary Report
  • Flt3 Itd Mutation
  • Flt3 Itd Signal Ratio (mutant: Wildtype)
  • Flt3 D835 Mutation
  • Clinical Details

  • Specimen Source
  • Preliminary Report
  • Npm1 Mutation
  • Clinical Details

  • Specimen Source
  • Preliminary Report
  • Cebpa Mutation
Frequently Asked Questions

This test identifies molecular abnormalities in Acute Myeloid Leukemia (AML) patients without major chromosomal changes.

Patients diagnosed with AML who require genetic profiling for targeted treatment should consider this test.

A bone marrow or blood sample undergoes genetic analysis.

Certain mutations can influence prognosis and treatment response.

Yes, through chemotherapy, targeted therapy, or stem cell transplants.

Test code

9303

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Bone MarrowOthers5 ML
Edta Whole BloodLavender Vacutainer8 ML

Specimen stability information

Bone Marrow, Edta Whole Blood

Collection instructions

Clinical History

Specimen rejection criteria

Test run frequency

'

Turn around time

7 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

ACUTE MYELOID LEUKEMIA (AML)

13500