Abstract
Cystic fibrosis (CF) is an orphan disease with increased morbidity and mortality, mainly due to chronic pulmonary infections. The symptoms and treatment are complex, and patients are followed at specialised CF centres. The exact treatment, and the segregation policies to avoid cross-infection from airway pathogens, vary between CF centres, including those in Scandinavian countries.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
