Literature DB >> 6775143

Three instances of neonatal death with hyperammonaemia, each resulting from a different cause.

T Palmer, V G Oberholzer, E A Burgess, S Mantagos.   

Abstract

We report here the results of a study of three unrelated patients, K., M. and R., each of whom died in the neonatal period in St Sophia's Children's Hospital, Athens, Greece, after a normal pregnancy and delivery. Liver functions tests and blood cultures gave normal results in each case and autopsy did not reveal any specific findings. All had gross hyperammonaemia and were considered to have possible urea cycle defects.

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Year:  1980        PMID: 6775143     DOI: 10.1007/bf02312532

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  4 in total

1.  Neonatal hyperammonaemia with complete absence of liver carbamyl phosphate synthetase activity.

Authors:  S Mantagos; S Tsagaraki; E A Burgess; V Oberholzer; T Palmer; J Sacks; S Baibas; T Valaes
Journal:  Arch Dis Child       Date:  1978-03       Impact factor: 3.791

Review 2.  Inherited hyperammonemic syndromes.

Authors:  Y E Hsia
Journal:  Gastroenterology       Date:  1974-08       Impact factor: 22.682

3.  Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings.

Authors:  J M Saudubray; C Marsac; C L Cathelineau; M Besson Leaud; J P Leroux
Journal:  Acta Paediatr Scand       Date:  1976-11

4.  A defect in pyruvate decarboxylase in a child with an intermittent movement disorder.

Authors:  J P Blass; J Avigan; B W Uhlendorf
Journal:  J Clin Invest       Date:  1970-03       Impact factor: 14.808

  4 in total

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