Journal of Inherited Metabolic Disease

, Volume 10, Issue 2, pp 198–199 | Cite as

Non-ketotic hyperglycinaemia: prenatal diagnosis and detection of heterozygotes with glycine/serine ratios

  • A. Jordá
  • M. Portolés
  • F. Bonilla-Musoles
  • L. Sweetman
  • W. L. Nyhan
Case Report

Keywords

Public Health Internal Medicine Metabolic Disease Prenatal Diagnosis 
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.
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References

  1. Carson, N. A. J. Non-ketotic hyperglycinaemia — A review of 70 patients.J. Inher. Metab. Dis. 5, Suppl. 2 (1982) 126–128Google Scholar
  2. García-Castro, J. M., Isales-Forsythe, C. M., Levy, H. L., Shih, V. E., Lao-Velez, E. R., González-Ríos, M. C. and Reyes de Torres, L. C. Prenatal diagnosis of nonketotic hyperglycinemia.N. Engl. J. Med. 306 (1982) 79–81Google Scholar
  3. Nyhan, W. L. Nonketotic hyperglycinemia. In Stanbury, J. B., Wyngaarden, J. E., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds.)The Metabolic Basis of Inherited Disease, 5th Edn., McGraw-Hill, New York, 1983, pp. 561–569Google Scholar

Copyright information

© SSIEM and MTP Press Limited 1987

Authors and Affiliations

  • A. Jordá
    • 1
  • M. Portolés
    • 1
  • F. Bonilla-Musoles
    • 2
  • L. Sweetman
    • 3
  • W. L. Nyhan
    • 3
  1. 1.Instituto de Investigaciones Citológicas de la Caja de Ahorros de ValenciaValenciaSpain
  2. 2.Department of GynaecologyHospital Clinico UniversitarioValenciaSpain
  3. 3.Department of PediatricsUniversity of CaliforniaSan Diego, La JollaUSA

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