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1 INTRODUCTION Primary ciliary dyskinesia (PCD) is a rare genetic disease, occurring between 1 in every 7000–10,000 live births in most communities, characterized by defects in the motile cilia lining the respiratory tract and other organs.1 In PCD, cilial ultrastructural deficiencies lead to poorly motile cilia, which, in turn, result in reduced mucous clearance in the lungs and upper airways.
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