Sleep Respiratory Disorders in Children and Adolescents with Cystic Fibrosis and Primary Ciliary Dyskinesia
Cystic fibrosis (CF) and primary ciliary dyskinesia (PCD) are genetic respiratory diseases featured by chronic upper and lower airway inflammation and infection, mainly due to impaired mucociliary clearance due to genetic mutations. Sleep is crucial to healthy children’s normal physical and psycholo...
Main Authors: | Maria Papale, Sara Manti, Santiago Presti, Federico Mollica, Giuseppe F. Parisi, Salvatore Leonardi |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-10-01
|
Series: | Children |
Subjects: | |
Online Access: | https://www.mdpi.com/2227-9067/10/10/1707 |
Similar Items
-
Changes in Sleep in Children and Adults with Cystic Fibrosis and Primary Ciliary Dyskinesia over Time and after CFTR Modulator Therapy
by: Malena Cohen-Cymberknoh, et al.
Published: (2023-12-01) -
Etiological Work-Up for Adults with Bronchiectasis: A Predictive Diagnostic Score for Primary Ciliary Dyskinesia and Cystic Fibrosis
by: Frederic Schlemmer, et al.
Published: (2021-08-01) -
The Short Term Influence of Chest Physiotherapy on Lung Function Parameters in Children With Cystic Fibrosis and Primary Ciliary Dyskinesia
by: Bjarne Vandervoort, et al.
Published: (2022-05-01) -
Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study
by: Marco Maglione, et al.
Published: (2017-04-01) -
Impaired Nitric Oxide Synthetase Activity in Primary Ciliary Dyskinesia—Data-Driven Hypothesis
by: Lisa Eggenkemper, et al.
Published: (2023-09-01)