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Article

Clinical and genetic spectrum of primary ciliary dyskinesia in Chinese patients: a systematic review.

Orphanet journal of rare diseases - 19 Jul 2022

Peng Bo, Gao Yong-Hua, Xie Jia-Qi, He Xiao-Wen, Wang Cong-Cong, Xu Jin-Fu, Zhang Guo-Jun

Abstract excerpt

BACKGROUND: Primary ciliary dyskinesia (PCD) represents a highly heterogenous disorder with extensive clinical and genetic patterns among populations of different geographic location and ethnic origin. However, data about Chinese patients are limited. We aimed to summarize the clinical and genetic spectrum of Chinese PCD patients based on all available literatures. METHODS: We searched Embase, Pubmed, Web of...

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Identifiers

PMID: 35854386
DOI: 10.1186/s13023-022-02427-1
PMCID: PMC9295413

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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