Chromosome Breakage Test - Fanconi's Anemia
- 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
CPT and Loinc codes
Department
- Cytogenetics
Turn around time
16 Working Days
Test run frequency
Every Day TIME - 07:00
Performing locations
1 labs across India
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.
Package price
₹8600
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₹8600