Abstract
An ear nose throat survey was carried out on 50 children aged 4 to 10 yr with cystic fibrosis. 10% were shown to be transiently deaf, associated with eustachian tube dysfunction. There were no confirmed cases of secretory otitis media. 10 children (20%) were found to have nasal polyps or gave a history of polypectomy. Though a high incidence of middle ear problems in children with cystic fibrosis has been reported from the USA, neither deafness nor secretory oritis media was found to be a problem in the group studied.
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CITATION STYLE
Taylor, B., Evans, J. N. G., & Hope, G. A. (1974). Upper respiratory tract in cystic fibrosis. Ear nose throat survey of 50 children. Archives of Disease in Childhood, 49(2), 133–136. https://doi.org/10.1136/adc.49.2.133
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