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
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References
Jones, A. and Bodmer, W. F. (1974). Our Future Inheritance: Choice or Chance. (London: Oxford University Press)
Whity, L. G. (1974). Screening for disease: definitions and criteria. Lancet, ii, 819
Smith, A. (1975). The Human Pedigree. ( London: George Allen and Unwin )
Cowie, V. (1972). Genetic counselling and social aspects of prenatal and new born screening. Ann. Clin.. Biochem., 9, 112
Department of Health and Social Security. (1969). Screening for early detection of phenylketonuria. HMSO (69) 72
Raine, D. N. (1974). Screening for disease: inherited metabolic disease Lancet, ii, 996
Guthrie, R. and Susi, A. (1963). A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants. Pediatrics, 32, 338
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
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
Hudson, F. P. and Hawcroft, J. (1975). M.R.C.—D.H.S.S. Phenylketonuria Newsletter No. 3
Nuffield Provincial Hospitals Trust. (1968). Screening in Medical Care. (London: Oxford University Press)
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
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
World Health Organization Scientific Group. (1968). Screening for Inborn Errors of Metabolism. WHO Tech. Rep. Ser., No. 401
Committee for the study of Inborn Errors of Metabolism. (1975). Genetic Screening Programs, Principles and Research. ( Washington: National Academy of Sciences )
Ratner, G. (1976). The coming of the second genetic code: eugenic abortion in the United Kingdom. This volume, p 119
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
Hudson, F. P. and Mordaunt,V. L. (1968). Opinions of health visitors and mother on screening for phenylketonuria. Med. Off. 120, 205
Holton, J. and Tyfield, L. (1974) The Child with Phenylketonuria. ( London: National Society for Mentally Handicapped Children )
Steele, S. J. and Goodwin, M. F. (1975). A pamphlet to answer patient’s questions. Lancet, ii, 822
Scriver, C. R., Clow, C. L. and Lamm, P. (1973). On the screening diagnosis and investigation of hereditary amino acidopathies. Clin. Biochem., 6, 142
Munro, T. A. (1947). Phenylketonuria: data on 47 British families. Ann. Eugenics, 14, 60
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
Wilson, J. M. G. and Junger, G. (1968). Principles and Practice of Screening for Disease. ( Geneva: World Health Organization )
Holland, W. W. (1974). Screening for disease: taking stock. Lancet, ii, 1494
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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
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DOI: https://doi.org/10.1007/978-94-011-6173-2_6
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