BETA THALASSEMIA FULL GENE SEQUENCING, EDTA BLOOD
Detects specific genetic mutations associated with beta thalassemia, a blood disorder that affects hemoglobin production. It helps diagnose and determine the severity of the condition.
BETA THALASSEMIA FULL GENE SEQUENCING, EDTA BLOOD Test in Vadodara Overview
No special preparations needed
- Specimen Source
- Preliminary Report
- Beta-thalassemia
The beta thalassemia mutation detection test identifies mutations in the HBB gene, responsible for beta thalassemia, a blood disorder that reduces hemoglobin production.
It is recommended for individuals with anemia, abnormal hemoglobin levels, or a family history of thalassemia.
A blood sample is analyzed using PCR or genetic sequencing to identify mutations in the HBB gene.
- Positive result: Confirms a beta thalassemia mutation.
- Negative result: No mutations detected in the HBB
Test code
2482
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 3 ML |
Specimen stability information
Edta Whole Blood
Specimen rejection criteria
Test run frequency
Every Day TIME - 09:30
Turn around time
12 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
Package price
₹7200
Need Help?
Talk to our health experts for guidance on tests, reports, or bookings.
WhatsApp to Book TestBETA THALASSEMIA FULL GENE SEQUENCING, EDTA BLOOD
₹7200