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Article

<i>DNAI1</i> Mutations Explain Only 2% of Primary Ciliary Dykinesia

1 Jan 2008

Abstract excerpt

BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare recessive hereditary disorder characterized by dysmotility to immotility of ciliated and flagellated structures. Its main symptoms are respiratory, caused by defective ciliary beating in the epithelium of the upper airways (nose, bronchi and paranasal sinuses). Impairing the drainage of inhaled microorganisms and particles leads to recurrent infections and...

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PMID: 18434704
DOI: 10.1159/000128567

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