Cystic Fibrosis Delta F508 Gene Mutation

Available viaHome Collection, Lab Visit

GenderMale & Female

Contains1 parameters

Earliest reports in8 Working Days

PreparationNo preparation 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

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

Cystic Fibrosis Delta F508 Gene Mutation

Package price

₹14000

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Cystic Fibrosis Delta F508 Gene Mutation

₹14000

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