Chromosome Breakage Test - Fanconi's Anemia
Overview of Chromosome Breakage Test - Fanconi's Anemia in Kottayam
What is the Fanconi’s anemia test?
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.
When is the Fanconi’s anemia test recommended?
It is recommended for individuals with symptoms such as bone marrow failure, congenital abnormalities, or a family history of FA.
How is the test performed?
A blood sample is analyzed using chromosomal breakage tests or molecular genetic testing to identify FA-related gene mutations.
What do the results indicate?
Positive result: Confirms a diagnosis of Fanconi anemia.
Negative result: Indicates no evidence of FA.
Test included
- Specimen
- Indications
- Cells Counted & Analysed
- Cells Karyotyped
- Karyotype
Doctor information
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.
Test price
₹8100
₹86006% offNeed Help?
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₹8100
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