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.
CHROMOSOME BREAKAGE TEST – FANCONI’S ANEMIA Test in Mangaluru Overview
No special preparations needed
- Specimen
- Indications
- Cells Counted & Analysed
- Cells Karyotyped
- Karyotype
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
| Specimen | Vacutainer | Volume |
|---|---|---|
| Heparin Whole Blood | Green Vacutainer | 5 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
Package price
₹8600
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₹8600