RANDOM CILIARY ORIENTATION - A CAUSE OF RESPIRATORY-TRACT DISEASE

被引:78
|
作者
RUTLAND, J
DEIONGH, RU
机构
[1] Respiratory Unit, Concord Hospital, Concord, Sydney
来源
NEW ENGLAND JOURNAL OF MEDICINE | 1990年 / 323卷 / 24期
关键词
D O I
10.1056/NEJM199012133232406
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The clinical manifestations of primary ciliary dyskinesia (PCD) — recurrent sinopulmonary infection and male sterility — have been attributed to defects in the ultrastructure of the central core (axoneme) of cilia and sperm tails. In the respiratory tract, these structural defects impair ciliary motility and coordination, resulting in reduced mucociliary clearance. Defective ciliary function and structure were first reported as a cause of recurrent respiratory disease by Afzelius and coworkers,1 , 2 who noted decreased ciliary motility in patients with Kartagener's syndrome and suggested the term immotile-cilia syndrome. Subsequent studies of ciliary motility and ultrastructure have revealed a range of patterns of. © 1990, Massachusetts Medical Society. All rights reserved.
引用
收藏
页码:1681 / 1684
页数:4
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