The Swiss Primary Ciliary Dyskinesia registry: objectives, methods and first results

The Swiss Primary Ciliary Dyskinesia registry: objectives, methods and first results

Primary ciliary dyskinesia (PCD) is a rare, hereditary, multiorgan disease caused by defects in the structure and function of motile cilia. It results in a wide range of clinical manifestations, most commonly in the upper and lower airways. Central data collection in national and international reg...

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Bibliographic Details
Main Authors: Myrofora Goutaki, Marc O. Eich, Florian S. Halbeisen, Juerg Barben, Carmen Casaulta, Christian Clarenbach, Gaudenz Hafen, Philipp Latzin, Nicolas Regamey, Romain Lazor, Stefan Tschanz, Maura Zanolari, Elisabeth Maurer, Claudia E. Kuehni, for the Swiss PCD Registry (CH-PCD) Working Group
Format: Article
Language:English
Published: SMW supporting association (Trägerverein Swiss Medical Weekly SMW) 2019-01-01
Series:Swiss Medical Weekly
Subjects:
Epidemiology
orphan diseases
patient registry
primary ciliary dyskinesia
Swiss Primary Ciliary Dyskinesia Registry
Online Access:https://www.smw.ch/index.php/smw/article/view/2562

Internet

https://www.smw.ch/index.php/smw/article/view/2562

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