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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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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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European Respiratory Society
2015
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| 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 |