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Disease characterization of people with cystic fibrosis and a minimal function mutation: Data from the Italian registry.

Pediatric pulmonology - 1 Oct 2021

Salvatore Donatello, Carnovale Vincenzo, Majo Fabio, Padoan Rita, Quattrucci Serena, Salvatore Marco, Taruscio Domenica, Amato Annalisa, Ferrari Gianluca, Campagna Giuseppe

Abstract excerpt

BACKGROUND: People with cystic fibrosis (pwCF) and a minimal function (MF) mutation are poorly characterized. The aim of this study was to evaluate the disease characteristics of adult and pediatric pwCF with a genotype including an MF mutation on the basis of 2018 data from the Italian CF Registry (ICFR). METHODS: This cross-sectional, descriptive analysis of CF disease characteristics included all of the pwCF...

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PMID: 34357699
DOI: 10.1002/ppul.25616

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