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Registries and collaborative studies for primary ciliary dyskinesia in Europe
Primary ciliary dyskinesia (PCD) is a rare inherited disease characterised by malfunctioning cilia leading to a heterogeneous clinical phenotype with many organ systems affected. There is a lack of data on clinical presentation, prognosis and effectiveness of treatments, making it mandatory to impro...
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| Main Authors: | , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
European Respiratory Society
2020-05-01
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| Colecção: | ERJ Open Research |
| Acesso em linha: | http://openres.ersjournals.com/content/6/2/00005-2020.full |
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