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

J. Shapiro, Adam; A. Zariwala, Maimoona; Ferkol, Thomas; D. Davis, Stephanie; D. Sagel, Scott; D. Dell, Sharon; Rosenfeld, Margaret; N. Olivier, Kenneth; Milla, Carlos; J. Daniel, Sam; J. Kimple, Adam; Manion, Michele; R. Knowles, Michael; W. Leigh, Margaret; the Genetic Disorders of Mucociliary Clearance Consortium, for

doi:10.1002/ppul.23304

Public

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

Shared by NobleBlocks on Sep 28, 2015 • 12:00 AM UTC

Authors:

Adam J. Shapiro

Maimoona A. Zariwala

Thomas Ferkol

Abstract

Summary 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 test...

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