Skip to main content

Abstract

The ‘good press’ accorded various diseases and their treatment by the medical correspondents of newspapers, magazines, radio and television has increased the awareness, knowledge and, partially, the understanding of medicine by the general public. Whilst raising the level of public acceptance of investigation and treatment, the media have raised the level of public expectation and the need for clear information from hospital and community medical services where illness or disorder affects themselves or their families. The scientific, social, ethical and legal implications of the rapid advances in the fields of genetics and biology have stimulated considerable discussion in the medical and lay press about hereditary disorders and screening procedures.1

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Jones, A. and Bodmer, W. F. (1974). Our Future Inheritance: Choice or Chance. (London: Oxford University Press)

    Google Scholar 

  2. Whity, L. G. (1974). Screening for disease: definitions and criteria. Lancet, ii, 819

    Google Scholar 

  3. Smith, A. (1975). The Human Pedigree. ( London: George Allen and Unwin )

    Google Scholar 

  4. Cowie, V. (1972). Genetic counselling and social aspects of prenatal and new born screening. Ann. Clin.. Biochem., 9, 112

    Google Scholar 

  5. Department of Health and Social Security. (1969). Screening for early detection of phenylketonuria. HMSO (69) 72

    Google Scholar 

  6. Raine, D. N. (1974). Screening for disease: inherited metabolic disease Lancet, ii, 996

    Google Scholar 

  7. Guthrie, R. and Susi, A. (1963). A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants. Pediatrics, 32, 338

    PubMed  CAS  Google Scholar 

  8. Scriver, C. R., Davies, E. and Cullen, A. M. (1964). Application of a simple micromethod to the screening of plasma for a variety of amino acidopathies. Lancet, ii, 230

    Google Scholar 

  9. Raine, D. N., Cooke, J. R., Andrews, W. A. and Mahon, D. F. (1972). Screening for inherited metabolic disease by plasma chromatography (Scriver) in a large city. Br. Med. J., 3, 7

    Article  PubMed  CAS  Google Scholar 

  10. Hudson, F. P. and Hawcroft, J. (1975). M.R.C.—D.H.S.S. Phenylketonuria Newsletter No. 3

    Google Scholar 

  11. Nuffield Provincial Hospitals Trust. (1968). Screening in Medical Care. (London: Oxford University Press)

    Google Scholar 

  12. Komrower, G. M., Fowler, B., Griffiths, M. J. and Lambert, A. M. (1968). A prospective community survey for aminoacidaemias. Proc. R. Soc. Med. 61, 294

    PubMed  CAS  Google Scholar 

  13. Sardharwalla, I. B., Komrower, G. M., Bridge, C. and Gordon, D. B. (1972). One-dimensional chromatography of plasma in Manchester. Ann. Clin. Biochem., 9, 126

    Google Scholar 

  14. World Health Organization Scientific Group. (1968). Screening for Inborn Errors of Metabolism. WHO Tech. Rep. Ser., No. 401

    Google Scholar 

  15. Committee for the study of Inborn Errors of Metabolism. (1975). Genetic Screening Programs, Principles and Research. ( Washington: National Academy of Sciences )

    Google Scholar 

  16. Ratner, G. (1976). The coming of the second genetic code: eugenic abortion in the United Kingdom. This volume, p 119

    Google Scholar 

  17. Raine, D. N. (1974). The need for a national policy for the management of inherited metabolic disease. In Raine, D. N. (ed.), Molecular Variants in Disease. J. Clin. Pathol., 27, ( Suppl.) (Roy. Coll. Path. ) 8

    Google Scholar 

  18. Hudson, F. P. and Mordaunt,V. L. (1968). Opinions of health visitors and mother on screening for phenylketonuria. Med. Off. 120, 205

    Google Scholar 

  19. Holton, J. and Tyfield, L. (1974) The Child with Phenylketonuria. ( London: National Society for Mentally Handicapped Children )

    Google Scholar 

  20. Steele, S. J. and Goodwin, M. F. (1975). A pamphlet to answer patient’s questions. Lancet, ii, 822

    Article  Google Scholar 

  21. Scriver, C. R., Clow, C. L. and Lamm, P. (1973). On the screening diagnosis and investigation of hereditary amino acidopathies. Clin. Biochem., 6, 142

    Article  PubMed  CAS  Google Scholar 

  22. Munro, T. A. (1947). Phenylketonuria: data on 47 British families. Ann. Eugenics, 14, 60

    Google Scholar 

  23. Fuller, R. N. and Shuman, J. B. (1974). Genetic divergence in relatives of PKU’s: low I.Q. correlation among normal siblings. Dev. Psychobiol., 7, 323

    Article  PubMed  CAS  Google Scholar 

  24. Wilson, J. M. G. and Junger, G. (1968). Principles and Practice of Screening for Disease. ( Geneva: World Health Organization )

    Google Scholar 

  25. Holland, W. W. (1974). Screening for disease: taking stock. Lancet, ii, 1494

    Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1977 The Society for the Study of Inborn Errors of Metabolism

About this chapter

Cite this chapter

May, E.D. (1977). Parent reaction to medical care and screening. In: Raine, D.N. (eds) Medico-Social Management of Inherited Metabolic Disease. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-6173-2_6

Download citation

  • DOI: https://doi.org/10.1007/978-94-011-6173-2_6

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-011-6175-6

  • Online ISBN: 978-94-011-6173-2

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics