Article

Clinical manifestations and genotype of primary ciliary dyskinesia diagnosed in Korea: a nationwide, multicenter, retrospective study

2022-05-17

Abstract excerpt

<h4>Background: </h4> Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder that leads to secondary ciliary dysfunction. PCD is a rare disease worldwide, and its data are limited in Korea. This study systematically evaluated the clinical symptoms, diagnostic characteristics, and treatment of pediatric PCD in Korea. <h4>Methods: </h4> The medical records of paediatric patients diagnosed with PCD...

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Literature Corpus work: 73844155-7a70-5baf-80ec-b3634643d956
DOI: 10.21203/rs.3.rs-1613158/v1

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