Rutman A, Cullinan P, Woodhead M, Cole P J, Wilson R
Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London.
Thorax. 1993 Jul;48(7):770-1. doi: 10.1136/thx.48.7.770.
Random ciliary orientation has recently been proposed as a variant of primary ciliary dyskinesia. We report a 12 year old boy with all the features of primary ciliary dyskinesia and absent nasal mucociliary clearance in whom repeated biopsies of the nasal epithelium showed normal ciliary beat frequency. The only abnormality discovered was disorientation of the central microtubules of his cilia.
随机纤毛定向最近被提出作为原发性纤毛运动障碍的一种变体。我们报告一名12岁男孩,具有原发性纤毛运动障碍的所有特征且鼻黏膜纤毛清除功能缺失,其鼻上皮的多次活检显示纤毛摆动频率正常。唯一发现的异常是其纤毛中央微管的定向异常。