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Journal of Inherited Metabolic Disease

, Volume 11, Issue 4, pp 427–428 | Cite as

Changes in phenylalanine tolerance while monitoring the dietetic treatment of pregnant women suffering from hyperphenylalaninaemia

  • J. Hyánek
  • H. Viletová
  • J. Soukup
  • J. Kobilková
  • M. Kubík
  • V. Kunová
Case Report

Keywords

Public Health Internal Medicine Pregnant Woman Metabolic Disease Phenylalanine 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Güttler, F. Hyperphenylalaninemia. Diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.Acta Paediat. Scand. 69 (1980) Suppl. 280Google Scholar
  2. Hyánek, J., Homolka, J., Trnka, J., Seemanová, E., Červenka, J., Třesohlavá, Z., Kapras, J., Doležal, A., Šráček, J., Vácha, V., Hoza, J., Lošan, F., Nevšísmalová, S., Malá, M. and Viletová, H. Results of screening for phenylalanine and other amino acid disturbances among pregnant women.J. Inher. Metab. Dis. 2 (1979) 59–63Google Scholar
  3. Lenke, R. R. and Levy, H. L. Maternal phenylketonuria and hyperphenylalaninemia. An international survey of outcome of untreated and treated pregnancies.N. Engl. J. Med. 303 (1980) 1202–1208Google Scholar
  4. Räihä, N. C. R. Phenylalanine hydroxylase in human liver during development.Pediatr. Res. 7 (1973) 1–4Google Scholar

Copyright information

© SSIEM and MTP Press Limited 1988

Authors and Affiliations

  • J. Hyánek
    • 1
  • H. Viletová
    • 1
  • J. Soukup
    • 1
  • J. Kobilková
    • 1
  • M. Kubík
    • 1
  • V. Kunová
    • 1
  1. 1.Department of Clinical Chemistry — Diagnostic Center for Inherited Disorders, and 2nd Clinic of Gynecology and ObstetricsCharles University Medical FacultyPragueCzechoslovakia

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