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原发性纤毛运动障碍与上气道疾病

Primary ciliary dyskinesia and upper airway diseases.

作者信息

Kennedy Marcus P, Ostrowski Lawrence E

机构信息

Cystic Fibrosis Pulmonary Research and Treatment Center, University of North Carolina, School of Medicine, 6125 Thurston Bowles Building, Chapel Hill, NC 27599, USA.

出版信息

Curr Allergy Asthma Rep. 2006 Nov;6(6):513-7. doi: 10.1007/s11882-006-0030-7.

Abstract

Primary ciliary dyskinesia (PCD) is a rare and difficult-to-diagnose disease with morbidity related to infections of the upper and lower respiratory tract. The disease is caused by mutations in genes that are required for proper ciliary function. The defect in ciliary function results in reduced or absent mucociliary clearance, thereby predisposing the affected individual to repeated bacterial infections. Recent advances in the understanding of the basic biology and function of the cilium have led to the identification of some of the genes that are mutated in cases of PCD. Further studies of this disease will likely lead to earlier diagnosis, better treatment, and improved outcomes.

摘要

原发性纤毛运动障碍(PCD)是一种罕见且难以诊断的疾病,其发病率与上、下呼吸道感染有关。该疾病由纤毛正常功能所需基因的突变引起。纤毛功能缺陷导致黏液纤毛清除功能减弱或缺失,从而使受影响个体易反复发生细菌感染。在对纤毛基本生物学和功能的理解方面的最新进展,已导致鉴定出一些在PCD病例中发生突变的基因。对该疾病的进一步研究可能会带来更早的诊断、更好的治疗和改善的预后。

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