[Disorders in mucociliary transport. Primary ciliary dyskinesia]
- PMID: 6367137
[Disorders in mucociliary transport. Primary ciliary dyskinesia]
Abstract
A survey is given of the mucociliary transport in the airways. Disturbances in rheologic qualities (viscosity and elasticity) of the mucuslayer may adversely influence mucociliary transport. This plays a role in cystic fibrosis and chronic bronchitis of other etiology. Disturbances in ciliary action can be secondary to for instance viral infections, inhalated substances and drugs. Inborn errors in the architecture of the cilia may cause immotility or ineffective motility of cilia, resulting in frequent airway infections. The clinical characteristics, diagnostic possibilities and a proposal for therapeutic measures are discussed.
Similar articles
-
Secondary ciliary dyskinesia in upper respiratory tract.Acta Otorhinolaryngol Belg. 2000;54(3):309-16. Acta Otorhinolaryngol Belg. 2000. PMID: 11082767 Review.
-
[Survey of diseases in the mucociliary system. Cilia are the first defense organs of the respiratory tract].Lakartidningen. 1995 Aug 30;92(35):3097-102, 3105. Lakartidningen. 1995. PMID: 7658761 Review. Swedish. No abstract available.
-
Testing ciliary activity in patients with chronic and recurrent infections of the upper airways: experiences in 68 cases.Laryngoscope. 1986 Sep;96(9 Pt 1):1029-33. Laryngoscope. 1986. PMID: 3528726
-
Ciliary function.Acta Otorhinolaryngol Belg. 2000;54(3):293-8. Acta Otorhinolaryngol Belg. 2000. PMID: 11082765
-
Function and ultrastructure of cilia in primary ciliary dyskinesia.Schweiz Med Wochenschr. 2000 May 13;130(19):699-704. Schweiz Med Wochenschr. 2000. PMID: 10846764
Cited by
-
Temporal and spatial distribution of ciliogenesis in the tracheobronchial airways of mice.Am J Physiol Lung Cell Mol Physiol. 2005 Sep;289(3):L454-9. doi: 10.1152/ajplung.00036.2005. Epub 2005 May 6. Am J Physiol Lung Cell Mol Physiol. 2005. PMID: 15879461 Free PMC article.