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Chromosome Breakage Test - Fanconi's Anemia

The chromosome breakage test for Fanconi’s anemia detects chromosomal instability characteristic of this genetic disorder. It helps diagnose Fanconi's anemia, a rare condition that leads to bone marrow failure and increases the risk of cancer.

Also known asStess Cytogenetics Chromosome Breakage Test – Fanconi’S Anemia Chromosome Breakage Test – Fanconi’S Anemia

Available via

Home Collection, Lab Visit

Contains

5 parameters

Earliest reports in

16 Working Days

Test details

Chromosome Breakage Test - Fanconi's Anemia Test in New Delhi Overview

Preparations

No special preparations needed

Test included
Chromosome Breakage Test - Fanconi's Anemia includes 5 parameters

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

The Fanconi’s anemia test detects mutations in genes responsible for Fanconi anemia (FA), a rare genetic disorder that affects bone marrow and increases the risk of cancer.

It is recommended for individuals with symptoms such as bone marrow failure, congenital abnormalities, or a family history of FA.

A blood sample is analyzed using chromosomal breakage tests or molecular genetic testing to identify FA-related gene mutations.

  • Positive result: Confirms a diagnosis of Fanconi anemia.
  • Negative result: Indicates no evidence of FA.

Test code

5812

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Heparin Whole BloodGreen Vacutainer5 ML

Specimen stability information

Heparin Whole Blood

Collection instructions

Specimen To Reach Us Within 24-48 Hrs + Clinical History, Speciman Of Age And Sex Mactched Control Sample Is Strongly Recommended. Sample Should Be Collect After 45 Days Of Blood Tranfuion.

Specimen rejection criteria

Test run frequency

Every Day TIME - 07:00

Turn around time

16 Working Days

Performing locations

Department

  • Cytogenetics

CPT and Loinc codes

Chromosome Breakage Test - Fanconi's Anemia

₹8600

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