Case Report: Primary ciliary dyskinesia due to CCNO mutations: a Chinese pediatric case series and literature review
Primary ciliary dyskinesia (PCD) is a hereditary disorder characterized by defects in cilia that impair mucociliary clearance. This study focuses on PCD caused by mutations in the Cyclin O (CCNO) gene and reports on three cases involving Chinese children. Case 1 was an 8-year-and-3-month-old boy who...
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Frontiers Media S.A.,
2024-09-01T00:00:00Z.
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