Skip to main content
SpringerLink
Log in
SpringerLink
Log in

Adverse Effects of Foods in Genetic Disorders

  • Chapter
Adverse Effects of Foods

  • 318 Accesses

Abstract

Most products of food metabolism have adverse effects on health if their concentrations in blood and extra- and intracellular fluids exceed narrow physiologic limits. Homeostasis, the maintenance of normal concentrations, is achieved by a vast number of genetically determined enzymatic processes that regulate digestion, absorption, transport, intermediate metabolism, and excretion.

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

Access this chapter

Log in via an institution
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

  • Ament, M. E., Perera, D. D., and Esther, L. J., 1973, Sucrase-isomaltase deficiency—a frequently misdiagnosed disease, J. Pediat. 83: 721–727.

    Article  CAS  Google Scholar 

  • Ament, M. E., 1979, Celiac Sprue in: Nelson, Textbook of Pediatrics, 11th ed. (V. Vaughn, J. McCay, and R. E. Behrman, eds.), p. 1083, W. B. Saunders, Philadelphia.

    Google Scholar 

  • Barry, R. E., and Read, A. E., 1973, Celiac disease and malignancy, Q. J. Med. 42: 665–675.

    CAS  Google Scholar 

  • Bayless, T. M., and Rosenzweig, N. S., 1966, A racial difference in incidence of lactase deficiency. J. Am. Med. Assoc. 197: 968–972.

    Article  CAS  Google Scholar 

  • Beutler, E., Baluda, M. C., Sturgeon, P., and Day, R. W., 1965, A new genetic abnormality resulting in galactose-1-phosphate uridyl transferase deficiency, Lancet 1: 353.

    Article  CAS  Google Scholar 

  • Beutler, E., 1970, L-dopa and favism, Blood 36: 523–525.

    Google Scholar 

  • Blackwell, B., 1963, Hypertensive crisis due to monoamine oxidase inhibitors, Lancet 2: 849.

    Article  CAS  Google Scholar 

  • Bottini, E. Lucarelli, P., Agostino, R., Palmarino, R., Businco, L., and Antagnoni, G., 1971, Favism: Association with erythrocyte acid phosphatase phenotype, Science 171: 409–411.

    Article  CAS  Google Scholar 

  • Danks, D. M., Cotton, R. G. H., and Schlesinger, P., 1979, Diagnosis of malignant hyperphenylalanemia, Arch. Dis. Child. 54: 329.

    Article  CAS  Google Scholar 

  • David, T. J., and Adjukiewicz, 1975, A family study of celiac disease, J. Med. Genet. 12: 79–82.

    Article  CAS  Google Scholar 

  • Falchuk, Z. M., Rogentine, G. M., and Strober, W., 1972, Predominance of histocompatibility antigen HL-A 8 in patients with gluten sensitive enteropathy, J. Clin. Invest. 51: 1602–1605.

    Article  CAS  Google Scholar 

  • Feingold, B. F., 1975, Hyperkinesis and learning disabilities linked to artificial food flavors and colors, Am. J. Nurs. 75: 797–803.

    CAS  Google Scholar 

  • Froesch, E. R., Wolf, H. P., Baitsch, H. H., Prader, A., and Labhart, A., 1963, Hereditary fructose intolerance: An inborn error of fructose metabolism, Am. J. Med. 34: 151.

    Article  CAS  Google Scholar 

  • Gray, G. M., 1978, Intestinal disaccharidase deficiencies and glucose-galactose malabsorption, in: The Metabolic Basis of Inherited Disease, 4th ed. ( J. B. Stanbury, J. B. Wyngaarden, and D. S. Frederickson, eds.), pp. 1526–1536, McGraw-Hill, New York.

    Google Scholar 

  • Hannington, E., 1967, Preliminary report of tyramine headache, Br. Med. J. 2: 250.

    Article  Google Scholar 

  • Henderson, W. R., and Raskin, N. H., 1972, “Hot dog” headache: Individual susceptibility to nitrate, Lancet 2:250.

    Google Scholar 

  • Holzel, A., Mereu, T., and Thomson, M. L., 1962, Severe lactose intolerance in infancy, Lancet 2: 1346.

    Article  CAS  Google Scholar 

  • Kattamis, A., Kyriazakou, M., and Chaidas, S., 1969, Favism, clinical and biochemical data, J. Med. Genet. 6: 34–41.

    Article  CAS  Google Scholar 

  • Kellermann, G., Luyten-Kellermann, M., and Shaw, C. R., 1973a, Genetic variation of aryl hydrocarbon hydroxylase in human lumphocytes, Am. J. Hum. Genet. 25: 327–331.

    CAS  Google Scholar 

  • Kellermann, G., Shaw, C. R., and Luyten-Kellermann, M., 1973b, Aryl hydrocarbon hydroxylase inductibility and bronchogenic carcinoma, N. Engl. J. Med. 289: 934–937.

    Article  CAS  Google Scholar 

  • La Du, B. N., 1978, Histidinemia, in: The Metabolic Basis of Inherited Disease, 4th ed. ( J. B. Stanbury, J. B. J. Wyngaarden, and D. S. Frederickson, eds.), pp. 317–327, McGraw-Hill, New York.

    Google Scholar 

  • Lindquist, B., Meuwisse, G. W., Melin, K., 1962, Glucose-galactose malabsorption, Lancet 2: 666.

    Article  Google Scholar 

  • Longdon, P. J., and Forsythe, W. I., 1979, Migraine in childhood. A review, Clin. Pediatr. 18: 353–356.

    Article  Google Scholar 

  • Mager, J., Glaser, G., Razin, A., Isak, C., Bien, S., and Noam, M., 1965, Metabolic effects of pyrimidines derived from glycosides on human erythrocytes deficient in glucose-6-phosphate dehydrogenase, Biochem. Biophys. Res. Comm. 20: 235–240.

    Article  CAS  Google Scholar 

  • McKusick, V. A., 1978, Mendelian Inheritance in Man, 5th ed., Johns Hopkins University Press, Baltimore, Maryland.

    Google Scholar 

  • Mentzler, W. C., and Collier, E., 1975, Hydrops fetalis associated with G-6-PD deficiency and maternal ingestion of fava beans and ascorbic acid, J. Pediatr. 86: 565–567.

    Article  Google Scholar 

  • Motulsky, A. G., 1964, Hereditary red cell traits and malaria, Am. J. Trop. Med. 13: 147–155.

    Google Scholar 

  • Paigen, B., Gurtoo, H. L., Minowada, J., Houten, L., Vincent, R., Paigen, K., Parker, N. E., Ward, E., and Hayner, N. T., 1977, Questionable relation of aryl hydrocarbon hydroxylase to lung cancer, N. Engl. J. Med. 297: 346–350.

    Article  CAS  Google Scholar 

  • Pollycove, M., 1978, Hemochromatosis, in: The Metabolic Basis of Inherited Disease, 4th ed. ( J. B. Stanbury, J. B. Wyngaarden, and D. S. Frederickson, eds.), pp. 1127–1164, McGraw-Hill, New York.

    Google Scholar 

  • Sandler, M., Yondim, M. B., and Harrington, E., 1974, A phenylethylamine oxidizing defect in migraine, Nature 250: 337–339.

    Article  Google Scholar 

  • Sansone, G., Piga, A. M., and Segni, G., 1958, El Favismo, Minerva Med., Torino, Italy.

    Google Scholar 

  • Sass-Kortsak, A. and Beam, A., 1978, Hereditary disorders of copper metabolism, in: The Metabolic Basis of Inherited Disease, 4th ed. ( J. B. Stanbury, J. B. Wyngaarden, and D. S. Frederickson, eds.), pp. 1098–1126, McGraw-Hill, New York.

    Google Scholar 

  • Segal, S., 1978, Disorders of galactose metabolism, in: The Metabolic Basis of Inherited Disease, 4th ed. ( J. B. Stanbury, J. B. Wyngaarden, and D. S. Frederickson, eds.), pp. 160–181, McGraw- Hill, New York.

    Google Scholar 

  • Schaumberg, H. H., Byck, R., Gerstl, R., and Mashman, J. H., 1969, Monosodium 1-glutamate: Its pharmacology and role in the Chinese Restaurant syndrome, Science 163: 826–828.

    Article  Google Scholar 

  • Smith, I., Clayton, B. E., and Wolff, O. H., 1975, new variant of phenylketonuria with progressive neurologic illness, Lancet 1: 1108–1111.

    Google Scholar 

  • Stammatoyannopoulis, G., Fraser, G. R., Motulsky, A. G., Fessas, P., Akrirakisn, A., and Papayannapoulou, T., 1966, On the familial predisposition of favism, Am. J. Hum Genet. 18: 253–263.

    Google Scholar 

  • Stanbury, J. B., Wyngaarden, J. B., and Frederickson, D. S. (eds.), 1978, The Metabolic Basis of Inherited Disease, 4th edition, McGraw-Hill, New York.

    Google Scholar 

  • Sunshine, P., and Kretschmer, N., 1964, Studies of small intestine during development III. Infantile diarrhea associated with intolerance to disaccharides, Pediatrics 34: 38–50.

    CAS  Google Scholar 

  • Szeinberg, A., Sheba, C., Hirshorn, N., and Bodonyi, E., 1957, Studies on erythrocytes in cases with past history of favism and drug induced hemolytic anemia, Blood 12: 603–616.

    CAS  Google Scholar 

  • Tarlov, A. R., Brewer, G. J., Carson, P. E., and Alving, A. S., 1962, Primaquine sensitivity. Glucose-6-Phosphate dehydrogenase deficiency and biological significance, Arch. Int. Med. 109: 209–234.

    CAS  Google Scholar 

  • Tourian, A. Y., and Sidbury, J. B., 1978, Phenylketonuria, in: The Metabolic Basis of Inherited Disease, 4th ed. ( J. B. Stanbury, J. B. Wyngaarden, and D. S. Frederickson, eds.), pp. 240–255, McGraw-Hill, New York.

    Google Scholar 

  • Wynder, E. L., 1979, Dietary habits and cancer epidemiology, Cancer 43: 1955–1961.

    Article  CAS  Google Scholar 

  • Wynder, E. L., 1980, Dietary factors related to breast cancer, Cancer 46: 899–904.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Department of Pediatrics, School of Medicine, Wright State University, Dayton, Ohio, 45404, USA

    Meinhard Robinow

Authors
  1. Meinhard Robinow
    View author publications

    You can also search for this author in PubMed Google Scholar

Editor information

Editors and Affiliations

  1. Population, Family and International Health Division, School of Public Health, University of California, Los Angeles, California, 90024, USA

    E. F. Patrice Jelliffe  & Derrick B. Jelliffe  & 

Rights and permissions

Reprints and permissions

Copyright information

© 1982 Plenum Press, New York

About this chapter

Cite this chapter

Robinow, M. (1982). Adverse Effects of Foods in Genetic Disorders. In: Jelliffe, E.F.P., Jelliffe, D.B. (eds) Adverse Effects of Foods. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-3359-3_29

Download citation

  • DOI: https://doi.org/10.1007/978-1-4613-3359-3_29

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-3361-6

  • Online ISBN: 978-1-4613-3359-3

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics

Search

Navigation