Hydrocephalus, bronchiectasis, and ciliary aplasia.

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Hydrocephalus and primary ciliary dyskinesia.

Primary ciliary dyskinesia was shown in a 12 year old boy with bronchiectasis who had developed hydrocephalus in the neonatal period. The possible relevance of his ciliary abnormality is discussed.

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Nasal ciliary function and mucociliary clearance were studied in patients with cystic fibrosis and in three control groups. Ciliary beat frequency and nasal clearance time were measured in groups of 10 subjects with cystic fibrosis, sinusitis and bronchiectasis and age and sex-matched control subjects. Ciliary beat frequency was also measured in normal subjects matched as bronchiectasis control...

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cilia in patients with primary ciliary dyskinesia, bronchiectasis, and in normal subjects

A reproducible technique, utilising a graphics tablet and a personal computer for measuring ciliary orientation from electron micrographs of ciliated epithelium, was assessed. Ciliary deviation was measured in 47 normal subjects (mean ciliary deviation ± 1 SD was 14-6 (3.30)), in eight patients with bronchiectasis and normal ciliary function (15.1 (6 50)), and in seven patients with primary cil...

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Orientation of respiratory tract cilia in patients with primary ciliary dyskinesia, bronchiectasis, and in normal subjects.

A reproducible technique, utilising a graphics tablet and a personal computer for measuring ciliary orientation from electron micrographs of ciliated epithelium, was assessed. Ciliary deviation was measured in 47 normal subjects (mean ciliary deviation +/- 1 SD was 14.6 (3.3 degrees)), in eight patients with bronchiectasis and normal ciliary function (15.1 (6.5 degrees], and in seven patients w...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 1990

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.65.5.543