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International consensus statement on routine blood testing in primary ciliary dyskinesia

Background Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by dysfunction of motile cilia. Symptoms include recurrent and chronic airway infections which can lead to deteriorating lung function and inflammatory destructive lung disease in the form of persistent atelectasis...

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Principais autores: Sarah Altaraihi, June K. Marthin, Pinelopi Anagnostopoulou, Mieke Boon, Siobhan B. Carr, Silvia Castillo-Corullón, Eleonora Dehlink, Damien M.S. Destouches, Jamie Duckers, Eric G. Haarman, Bülent Karadag, Christina Kavouridou, Michael R. Loebinger, Bernard Maitre, Henryk Mazurek, Lucy Morgan, Heymut Omran, Ugur Ozcelik, Daniel Peckam, Massimo Pifferi, Petr Pohunek, Tavs Qvist, Johanna Raidt, Phillipe Reix, Felix C. Ringshausen, Phil Robinson, Evie Robson, Jobst Röhmel, Francesca Santamaria, Anne Schlegtendal, Nicola Ullmann, Woolf Walker, Panayiotis Yiallouros, Guillaume Thouvenin, Suzanne Crowley, Kim G. Nielsen
Formato: Artigo
Idioma:Inglês
Publicado em: European Respiratory Society 2025-06-01
coleção:ERJ Open Research
Acesso em linha:http://openres.ersjournals.com/content/11/3/01071-2024.full
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