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. 1991 May;28(5):322–324. doi: 10.1136/jmg.28.5.322

What do young people think about screening for cystic fibrosis?

E Cobb 1, S Holloway 1, R Elton 1, J A Raeburn 1
PMCID: PMC1016850  PMID: 1865469

Abstract

We investigated the knowledge of cystic fibrosis and the views about neonatal and carrier screening in 216 school students aged 14 to 16 years. This work was completed before the published identification of the cystic fibrosis gene in September 1989. Although initial knowledge of cystic fibrosis was low (only 17% of the students knew that the disease affected the lungs), there was good recall of basic information about cystic fibrosis and of recessive inheritance after a brief lecture. A total of 86% considered that carrier detection should be offered routinely and 88% felt that an offer of prenatal diagnosis for cystic fibrosis should be made if both prospective parents were known to be carriers. We believe that pilot studies of cystic fibrosis carrier screening in schools should be undertaken.

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Selected References

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  1. Bak-Christensen A., Dimo B., Samson D., Wille-Jørgensen P. Cutaneous reactions in relation to the use of 'TED'-stockings. Lancet. 1989 Dec 2;2(8675):1346–1346. doi: 10.1016/s0140-6736(89)91962-4. [DOI] [PubMed] [Google Scholar]
  2. Kerem B., Rommens J. M., Buchanan J. A., Markiewicz D., Cox T. K., Chakravarti A., Buchwald M., Tsui L. C. Identification of the cystic fibrosis gene: genetic analysis. Science. 1989 Sep 8;245(4922):1073–1080. doi: 10.1126/science.2570460. [DOI] [PubMed] [Google Scholar]
  3. McIntosh I., Lorenzo M. L., Brock D. J. Frequency of delta F508 mutation on cystic fibrosis chromosomes in UK. Lancet. 1989 Dec 9;2(8676):1404–1405. doi: 10.1016/s0140-6736(89)92025-4. [DOI] [PubMed] [Google Scholar]
  4. Mouzouras M., Camba L., Ioannou P., Modell B., Constantinides P., Gale R. Thalassaemia as a model of recessive genetic disease in the community. Lancet. 1980 Sep 13;2(8194):574–578. doi: 10.1016/s0140-6736(80)92003-6. [DOI] [PubMed] [Google Scholar]
  5. Riordan J. R., Rommens J. M., Kerem B., Alon N., Rozmahel R., Grzelczak Z., Zielenski J., Lok S., Plavsic N., Chou J. L. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989 Sep 8;245(4922):1066–1073. doi: 10.1126/science.2475911. [DOI] [PubMed] [Google Scholar]
  6. Scriver C. R., Bardanis M., Cartier L., Clow C. L., Lancaster G. A., Ostrowsky J. T. Beta-thalassemia disease prevention: genetic medicine applied. Am J Hum Genet. 1984 Sep;36(5):1024–1038. [PMC free article] [PubMed] [Google Scholar]
  7. Stewart A. D. Screening for cystic fibrosis. Nature. 1989 Oct 26;341(6244):696–696. doi: 10.1038/341696b0. [DOI] [PubMed] [Google Scholar]
  8. Ten Kate L. P., Tijmstra T. Carrier screening for cystic fibrosis. Lancet. 1989 Oct 21;2(8669):973–974. doi: 10.1016/s0140-6736(89)90975-6. [DOI] [PubMed] [Google Scholar]
  9. Williamson R., Allison M. E., Bentley T. J., Lim S. M., Watson E., Chapple J., Adam S., Boulton M. Community attitudes to cystic fibrosis carrier testing in England: a pilot study. Prenat Diagn. 1989 Oct;9(10):727–734. doi: 10.1002/pd.1970091008. [DOI] [PubMed] [Google Scholar]
  10. Zeesman S., Clow C. L., Cartier L., Scriver C. R. A private view of heterozygosity: eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal. Am J Med Genet. 1984 Aug;18(4):769–778. doi: 10.1002/ajmg.1320180424. [DOI] [PubMed] [Google Scholar]

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