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Article

Primary Ciliary Dyskinesia: A Clinical Review.

Cells - 4 Jun 2024

Despotes Katherine A, Zariwala Maimoona A, Davis Stephanie D, Ferkol Thomas W

Abstract excerpt

Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous, motile ciliopathy, characterized by neonatal respiratory distress, recurrent upper and lower respiratory tract infections, subfertility, and laterality defects. Diagnosis relies on a combination of tests for confirmation, including nasal nitric oxide (nNO) measurements, high-speed videomicroscopy analysis (HSVMA), immunofluorescent staining,...

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Identifiers

PMID: 38891105
DOI: 10.3390/cells13110974
PMCID: PMC11171568

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