CYSTIC FIBROSIS,IRT (NEONATAL SCREEN) DRIED BLOOD SPOT (O.S)

Requirements

Sample Required Serum
Preperations Required Clinical history, metabolic disorders or inborn errors of metabolsim suspicion or provisional diagnosis of clincian required fasting recommended not mandatory. Amino acid supplementation or medications needs to stoped based on physician recommendations
Gender Male & Female
Age Group 0 - 99 Years
Collection AtHome & Lab

₹ 495

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1 Observations included

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CYSTIC FIBROSIS,IRT (NEONATAL SCREEN) DRIED BLOOD SPOT (O.S)

Observations Included

10,000+ Tests Done

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Overview

Cystic fibrosis (CF), in the classic form, is a severe autosomal recessive disorder characterized by a varied degree of chronic obstructive lung disease and pancreatic enzyme insufficiency. o date, over 1500 variants have been described within the CF gene, named cystic fibrosis transmembrane conductance regulator (CFTR). The most common variant, deltaF508, accounts for approximately 67% of the variants worldwide.