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导致原发性纤毛运动障碍的中央微管发育不全。

Central microtubular agenesis causing primary ciliary dyskinesia.

作者信息

Stannard Wendy, Rutman Andrew, Wallis Colin, O'Callaghan Chris

机构信息

Division of Child Health, Institute of Lung Health, Department of Infection, Immunity, and Inflammation, University of Leicester, UK.

出版信息

Am J Respir Crit Care Med. 2004 Mar 1;169(5):634-7. doi: 10.1164/rccm.200306-782OC.

Abstract

Primary ciliary dyskinesia is an autosomal recessive disorder characterized by chronic upper and lower respiratory tract symptoms. We report the diagnosis of primary ciliary dyskinesia associated with a circular ciliary beat pattern in three siblings. This beat pattern is consistent with a ciliary transposition defect, where a peripheral microtubule doublet is transposed to the center of the ciliary axoneme to replace the absent central microtubule pair. However, in these siblings, ultrastructural analysis of the cilia revealed an absence of the central microtubule pair only. This variant of transposition with a circular ciliary beat pattern has not been described previously. In addition, this defect, together with the transposition defect, may help explain the mechanism of the circular beat pattern and also the absence of situs inversus in these patients.

摘要

原发性纤毛运动障碍是一种常染色体隐性疾病,其特征为慢性上、下呼吸道症状。我们报告了三例患有原发性纤毛运动障碍且伴有环状纤毛摆动模式的同胞兄妹的诊断情况。这种摆动模式与纤毛转位缺陷一致,即外周微管二联体转位至纤毛轴丝中心以替代缺失的中央微管对。然而,在这些同胞兄妹中,纤毛的超微结构分析仅显示中央微管对缺失。此前尚未描述过这种伴有环状纤毛摆动模式的转位变体。此外,这种缺陷与转位缺陷一起,可能有助于解释环状摆动模式的机制以及这些患者中内脏反位的缺失情况。

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