Advertisement

European Journal of Pediatrics

, Volume 155, Issue 11, pp 992–992 | Cite as

Microcephaly and maternal phenylketonuria

  • A. Superti-Furga
  • B. Steinmann
  • G. Duc
  • R. Gitzelmann
Letters to the Editors

Keywords

Public Health Phenylketonuria Microcephaly Maternal Phenylketonuria 
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.

Abbreviation

PKU

phenylketonuria

References

  1. 1.
    Gungor N, Tokath A, Coskun T, Özguc M, Özalp I (1996) Microcephaly in a hyperphenylalaninemic infant leading to the diagnosis of maternal hyperphenylalaninemia. Eur J Pediatr 155:257–258Google Scholar
  2. 2.
    Superti-Furga A, Steinmann B, Due G, Gitzelmann R (1991) Maternal phenylketonuria in cousins caused by mild, unrecognized phenylketonuria in their mothers homozygous for the phenylalanin hydroxylase Arg-261-Gln mutation. Eur J Pediatr 150:493–497Google Scholar

Copyright information

© Springer-Verlag 1996

Authors and Affiliations

  • A. Superti-Furga
    • 1
  • B. Steinmann
    • 1
  • G. Duc
    • 2
  • R. Gitzelmann
    • 1
  1. 1.Division of Metabolic and Molecular Diseases, Department of PaediatricsUniversity of ZurichZurichSwitzerland
  2. 2.Division of Neonatology, Department of PaediatricsUniversity of ZurichZurichSwitzerland

Personalised recommendations