Abstract
We report a questionnaire survey of 216 adults (aged 16—68) attending the dental hospital in Newcastle. This was undertaken to provide a representative assessment of the level of knowledge in the community of cystic fibrosis and attitudes towards testing for carrier status. Knowledge of inheritance and symptomatology of the condition was scored and found to be less than previously reported in selected population groups. In the majority the source of information reported was the mass media; only 27 respondents had any contact with an affected individual. The questionnaire provided information about the inheritance and effects of cystic fibrosis. Three-quarters of the respondents accepted the idea of carrier testing for themselves, which included most of those of reproductive age, and all considerd that testing should be available to those planning a family. General practice surgeries were the most favoured venue for testing. The implications of these findings for those involved in the planning of population screening programmes are considered.
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Contributor Information
D. Magnay, Senior Clinical Medical Officer Northern Region Genetics Service, Newcastle upon Tyne
O. Wilson, Genetics Associate Northern Region Genetics Service, Newcastle upon Tyne
S. El Hait, MSc Student Northern Region Genetics Service, Newcastle upon Tyne
M. Balhamar, MSc Student Northern Region Genetics Service, Newcastle upon Tyne
J. Burn, Professor of Clinical Genetics Northern Region Genetics Service, Newcastle upon Tyne