CYSTIC FIBROSIS DELTA F508 GENE MUTATION
Detects the Delta F508 mutation in the CFTR gene, which is the most common mutation associated with cystic fibrosis, a genetic disorder that affects the lungs and digestive system.
CYSTIC FIBROSIS DELTA F508 GENE MUTATION Test in Vadodara Overview
No special preparations needed
- Cystic Fibrosis Delta F508 Mutation
This genetic test detects the Delta F508 mutation in the CFTR gene, the most common cause of cystic fibrosis (CF).
Newborns, individuals with CF symptoms, or those with a family history of cystic fibrosis should take this test.
A blood or saliva sample is analyzed for the Delta F508 mutation.
A positive result suggests CF or carrier status, requiring further testing.
No cure exists, but treatments like airway clearance therapy and medications can help manage symptoms.
Test code
RD1446
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 2 ml |
Specimen stability information
Edta Whole Blood
Collection instructions
Clinical History
Specimen rejection criteria
Test run frequency
Every Day TIME - 10:30
Turn around time
8 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
Package price
₹14000
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₹14000