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

Donatello SalvatoreVincenzo CarnovaleFabio MajoRita F PadoanSerena QuattrucciMarco SalvatoreDomenica TaruscioAnnalisa AmatoGianluca FerrariGiuseppe Campagna
Published in: Pediatric pulmonology (2021)
The findings of this descriptive analysis highlight the disease characteristics of pwCF with an MF-including genotype in Italy. The considered clinical outcomes of the pwCF with an F/MF genotype were not generally different from those of pwCF with an F/F genotype, but the patients with an MF/no-F genotype generally had a milder phenotype.
Keyphrases
  • cystic fibrosis
  • pseudomonas aeruginosa
  • electronic health record
  • lung function
  • data analysis
  • air pollution
  • deep learning