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.

Also known asCystic Fibrosis Delta F508 Gene Mutation Cystic Fibrosis Delta F508 Gene Mutation

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

8 Working Days

Test details

Cystic Fibrosis Delta F508 Gene Mutation Test in Jodhpur Overview

Preparations

No special preparations needed

Test included
Cystic Fibrosis Delta F508 Gene Mutation includes 1 parameter

  • Cystic Fibrosis Delta F508 Mutation
Frequently Asked Questions

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
SpecimenVacutainerVolume
Edta Whole BloodLavender Vacutainer2 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

Cystic Fibrosis Delta F508 Gene Mutation

14000

Health Checkup Category

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