SIDC

Cystic Fibrosis Mutation Detection - CFTR

Commonly Known As:

Cystic Fibrosis (deltaF508) CFTR mutation CFTR mutation CFTR Mutation Detection DeltaF508 ∆F508

Rs.6999 Rs.13998
(50% off)

Cystic fibrosis (CF), a.k.a mucoviscidosis, is a disorder that affects mainly the lungs but also the pancreas, liver, kidneys, and intestine. Cystic fibrosis is caused by a mutation in the gene Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). This test detects the most common CFTR mutation - ΔF508 which is a deletion of 3 nucleotides which results in a loss of the amino acid phenylalanine (F) at the 508th position on the protein. This mutation accounts for 2/3 of Cystic Fibrosis cases worldwide.

Test Preparation :

No Special Preparation. Informed Consent Required.

Reporting TAT :

Same Day

Specialisation(S) :

Test parameters includes :

Cystic Fibrosis (deltaF508) CFTR mutation

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Cystic Fibrosis Mutation Detection - CFTR

Cystic Fibrosis (deltaF508) CFTR mutation 1 Tests ▲

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