Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, rare lung disease resulting in chronic oto‐sino‐pulmonary disease in both children and adults. Many physicians incorrectly diagnose PCD or eliminate PCD from their differential diagnosis due to inexperience with diagnostic testing meth...

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Enregistré dans:
Détails bibliographiques
Publié dans:Pediatr Pulmonol
Auteurs principaux: Shapiro, Adam J., Zariwala, Maimoona A., Ferkol, Thomas, Davis, Stephanie D., Sagel, Scott D., Dell, Sharon D., Rosenfeld, Margaret, Olivier, Kenneth N., Milla, Carlos, Daniel, Sam J., Kimple, Adam J., Manion, Michele, Knowles, Michael R., Leigh, Margaret W.
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2015
Sujets:
State of the Art
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4912005/
https://ncbi.nlm.nih.gov/pubmed/26418604
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ppul.23304
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