Primary ciliary dyskinesia

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Key Points

The aim is to improve awareness and diagnosis of primary ciliary dyskinesia (PCD), particularly in pediatric populations.
Review of clinical features and diagnostic tests for PCD in children.
Analysis of genetic prevalence, particularly in Canadian Indigenous populations.
Discussion of therapeutic strategies and management protocols for PCD.
Diagnostic testing involving nasal nitric oxide and genetic analysis shows promise for improved PCD identification.
Prevalence of PCD is markedly higher in certain Indigenous populations, necessitating targeted screening.
A variety of symptoms are highlighted as critical for timely diagnosis, improving overall patient management.

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Review outlines diagnosis and management of primary ciliary dyskinesia in children, suggesting better screening methods for timely care.

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Lavoie et al. (2025) studied this question.

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