Literature DB >> 2919871

Transient neonatal hyperglycinemia.

R Schiffmann1, E M Kaye, J K Willis, D Africk, M Ampola.   

Abstract

Two patients with neonatal seizures and subsequent normal neurological development were found to have nonketotic hyperglycinemia. In both patients, hyperglycinemia resolved at 6 weeks of age. After cerebrospinal fluid glycine levels were normalized, the seizures stopped completely in one child and were markedly improved in the other. The possible mechanisms for the hyperglycinemia are discussed.

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Year:  1989        PMID: 2919871     DOI: 10.1002/ana.410250218

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  4 in total

1.  A false hyperglycinaemia.

Authors:  P Parvy; J Bardet; D Rabier; J Nedellec; P Kamoun
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

2.  Localized proton MR spectroscopic detection of nonketotic hyperglycinemia in an infant.

Authors:  C G Choi; H K Lee; J H Yoon
Journal:  Korean J Radiol       Date:  2001 Oct-Dec       Impact factor: 3.500

3.  Non-ketotic hyperglycinaemia: a therapeutic approach.

Authors:  I Apostolidou; C Papagaroufalis; H Michelakakis; C J Stephanidis; M Xanthou
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

Review 4.  Metabolic etiologies in West syndrome.

Authors:  Seda Salar; Solomon L Moshé; Aristea S Galanopoulou
Journal:  Epilepsia Open       Date:  2018-03-14
  4 in total

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