Phenotype of children with inconclusive cystic fibrosis diagnosis after newborn screening.

Anne MunckAurélie BourmaudGabriel BellonPaul PicqPhilip M Farrellnull null

Published in: Pediatric pulmonology (2020)

The matched CRMS/CFSPID and CF cohorts showed differences in outcomes. By a mean age of 7.6 years, a high proportion of the CRMS/CFSPID cohort converted to CF. Our results highlight that monitoring at CF clinics until at least 6 years is needed as well as further studies.

Keyphrases

cystic fibrosis
pseudomonas aeruginosa
lung function
primary care
young adults
type diabetes
case control
metabolic syndrome
weight loss