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

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

Abstract 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 g...

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Bibliographic Details
Main Authors: Bo Peng, Yong-hua Gao, Jia-qi Xie, Xiao-wen He, Cong-cong Wang, Jin-fu Xu, Guo-jun Zhang
Format: Article
Language:English
Published: BMC 2022-07-01
Series:Orphanet Journal of Rare Diseases
Subjects:
PCD
Systematic review
Genotype
Phenotype
Cilia
Online Access:https://doi.org/10.1186/s13023-022-02427-1

Internet

https://doi.org/10.1186/s13023-022-02427-1

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