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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 |
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author | de Benedictis, Fernando M. |
author_facet | de Benedictis, Fernando M. |
author_sort | de Benedictis, Fernando M. |
collection | PubMed |
description | 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 nearly 50% of cases. |
format | Online Article Text |
id | pubmed-4487373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-44873732015-08-24 GPs Meet Rare Lung Disorders Task Force factsheet: primary ciliary dyskinesia de Benedictis, Fernando M. Breathe (Sheff) Expert Opinion 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 nearly 50% of cases. European Respiratory Society 2015-06 /pmc/articles/PMC4487373/ /pubmed/26306119 http://dx.doi.org/10.1183/20734735.112215 Text en ©ERS 2015 http://creativecommons.org/licenses/by-nc/4.0/ Breathe articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0 (http://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Expert Opinion de Benedictis, Fernando M. GPs Meet Rare Lung Disorders Task Force factsheet: primary ciliary dyskinesia |
title | GPs Meet Rare Lung Disorders Task Force factsheet: primary ciliary dyskinesia |
title_full | GPs Meet Rare Lung Disorders Task Force factsheet: primary ciliary dyskinesia |
title_fullStr | GPs Meet Rare Lung Disorders Task Force factsheet: primary ciliary dyskinesia |
title_full_unstemmed | GPs Meet Rare Lung Disorders Task Force factsheet: primary ciliary dyskinesia |
title_short | GPs Meet Rare Lung Disorders Task Force factsheet: primary ciliary dyskinesia |
title_sort | gps meet rare lung disorders task force factsheet: primary ciliary dyskinesia |
topic | Expert Opinion |
url | 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 |
work_keys_str_mv | AT debenedictisfernandom gpsmeetrarelungdisorderstaskforcefactsheetprimaryciliarydyskinesia |