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了解原发性纤毛运动障碍。

Understanding primary ciliary dyskinesia.

作者信息

Ferkol Thomas

机构信息

Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.

出版信息

Pediatr Pulmonol. 2025 Mar;60 Suppl 1:S86-S87. doi: 10.1002/ppul.27360. Epub 2024 Oct 28.

Abstract

Primary ciliary dyskinesia (PCD) is a rare, inherited disease characterized by impaired motile ciliary function leading to chronic sinopulmonary disease, persistent middle ear effusions, laterality defects, and subfertility. Over fifty PCD-associated genes have also been identified, which have provided new insights into the processes involved into ciliary assembly, structure, and function. Historically, the diagnosis of PCD was based on the presence of ultrastructural defects in the ciliary axoneme but with identification of a growing number of disease-associated genes, genetic testing has become a first-line diagnostic tool. Other approaches have also evolved, that have improved our diagnostic capabilities. Treatments for PCD have lagged, and though our growing understanding of the genetic and pathophysiological bases of the disease of PCD may yield to better therapeutic strategies.

摘要

原发性纤毛运动障碍(PCD)是一种罕见的遗传性疾病,其特征是运动性纤毛功能受损,导致慢性鼻窦肺部疾病、持续性中耳积液、左右不对称缺陷和生育力低下。五十多个与PCD相关的基因也已被确定,这为纤毛组装、结构和功能所涉及的过程提供了新的见解。从历史上看,PCD的诊断基于纤毛轴丝超微结构缺陷的存在,但随着越来越多疾病相关基因的发现,基因检测已成为一线诊断工具。其他方法也有所发展,提高了我们的诊断能力。PCD的治疗一直滞后,尽管我们对PCD疾病的遗传和病理生理基础的日益了解可能会产生更好的治疗策略。

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