GPs Meet Rare Lung Disorders Task Force factsheet: primary ciliary dyskinesia

Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive disease of abnormalities of ciliary structure and function. The result is impaired mucociliary clearance, causing a variety of respiratory symptoms, and likely progression to bronchiectasis in most cases. Situs anomalies are present in...

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Detalles Bibliográficos
Autor principal: de Benedictis, Fernando M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2015
Materias:
Expert Opinion
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487373/
https://www.ncbi.nlm.nih.gov/pubmed/26306119
http://dx.doi.org/10.1183/20734735.112215

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487373/
https://www.ncbi.nlm.nih.gov/pubmed/26306119
http://dx.doi.org/10.1183/20734735.112215

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