Cystic Fibrosis Delta F508 Gene Mutation
Overview of Cystic Fibrosis Delta F508 Gene Mutation in Pathanamthitta
What is the Cystic Fibrosis Delta F508 Gene Mutation test?
This genetic test detects the Delta F508 mutation in the CFTR gene, the most common cause of cystic fibrosis (CF).
Who should take this test?
Newborns, individuals with CF symptoms, or those with a family history of cystic fibrosis should take this test.
How is the test performed?
A blood or saliva sample is analyzed for the Delta F508 mutation.
What do positive results indicate?
A positive result suggests CF or carrier status, requiring further testing.
Is there a cure for cystic fibrosis?
No cure exists, but treatments like airway clearance therapy and medications can help manage symptoms.
Test included
- Cystic Fibrosis Delta F508 Mutation
Doctor information
Test code
RD1446
CPT and Loinc codes
Department
- Advanced Molecular Diagnostics R&d
Turn around time
8 Working Days
Test run frequency
Every Day TIME - 10:30
Performing locations
1 labs across India
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
Test price
₹13790
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₹13790