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...

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Detalles Bibliográficos
Autores principales: Papale, Maria, Manti, Sara, Presti, Santiago, Mollica, Federico, Parisi, Giuseppe F., Leonardi, Salvatore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605080/
https://www.ncbi.nlm.nih.gov/pubmed/37892370
http://dx.doi.org/10.3390/children10101707

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605080/
https://www.ncbi.nlm.nih.gov/pubmed/37892370
http://dx.doi.org/10.3390/children10101707

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