Respiratory Aspects of Primary Ciliary Dyskinesia.


Journal

Clinics in chest medicine
ISSN: 1557-8216
Titre abrégé: Clin Chest Med
Pays: United States
ID NLM: 7907612

Informations de publication

Date de publication:
Sep 2024
Historique:
medline: 29 7 2024
pubmed: 29 7 2024
entrez: 28 7 2024
Statut: ppublish

Résumé

This review article explores the respiratory aspects of primary ciliary dyskinesia (PCD), a rare, heterogenous, genetic disorder characterized by impaired motile ciliary function. It discusses the clinical diagnosis and management strategies for PCD-related respiratory disease, including chronic sinusitis, otitis media with effusion, recurrent pneumonia, and bronchiectasis. The review emphasizes the need for a multidisciplinary approach to optimize care and clinical trials to improve outcomes in individuals with PCD, highlighting the importance of accurate diagnosis.

Identifiants

pubmed: 39069333
pii: S0272-5231(24)00022-4
doi: 10.1016/j.ccm.2024.02.020
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

717-728

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure The authors declare no conflicts of interest related to this article.

Auteurs

Wilfredo De Jesús-Rojas (W)

Department of Pediatrics & Basic Science, Ponce Health Sciences University, Ponce, Puerto Rico, PR 00716, USA.

Adam J Shapiro (AJ)

The Research Institute of the McGill University Health Centre, 2155, rue Guy, 5e étage, Montreal, QC, Canada H3H 2R9.

Amelia Shoemark (A)

Division of Molecular and Clinical Medicine, University of Dundee, Ninewells Hospital and Medical School, Dundee, UK; PCD Service, Royal Brompton Hospital, London, UK. Electronic address: a.shoemark@dundee.ac.uk.

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Classifications MeSH