Genetic Variants Supporting the Diagnosis of Primary Ciliary Dyskinesia in Japan

ABSTRACT Primary ciliary dyskinesia (PCD; OMIM 244400) is a rare genetic disorder affecting motile cilia and is characterized by impaired mucociliary clearance in the airway epithelium that leads to chronic oto‐sinopulmonary manifestations. To date, over 50 PCD‐causing genes have been identified, with these genes and their variants varying globally across populations. We performed targeted resequencing of 42 PCD‐causative genes in 150 Japanese patients suspected of having PCD and identified pathogenic or likely pathogenic variants in 51 patients. Among these, 24 patients exhibited a homozygous deletion of DRC1 exons 1–4, the most common cause of PCD in Japan. The allele frequency of this deletion was estimated at 0.0034 (95% CI: 0.0025–0.0044), based on bioinformatic analysis of 7906 whole‐genome sequences from the general Japanese population. Additionally, RNA sequencing of nasal samples supplemented in silico variant predictions, aiding in the identification of causative variants. Considering potential ethnic differences, it is essential to accumulate global data on these variants and their functional impacts.