Literature DB >> 8158601

Glutathione synthetase deficiency: a family report.

R K Pejaver1, A H Watson.   

Abstract

Glutathione synthetase deficiency is a rare inborn error of metabolism. Low levels of and at times unstable molecules of glutathione synthetase leads to glutathione deficiency affecting various systems of the body. The inheritance is thought to be of autosomal recessive variety. We diagnosed the condition in a neonate and proceeded to investigate the family. The results are discussed below.

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Year:  1994        PMID: 8158601      PMCID: PMC1294405          DOI: 10.1177/014107689408700321

Source DB:  PubMed          Journal:  J R Soc Med        ISSN: 0141-0768            Impact factor:   18.000


  4 in total

1.  Erythrocyte glutathione synthetase in 5-oxoprolinuria: kinetic studies of the mutant enzyme and detection of heterozygotes.

Authors:  A Larsson; R Zetterström; H Hörnell; U Porath
Journal:  Clin Chim Acta       Date:  1976-11-15       Impact factor: 3.786

2.  5-Oxoprolinuria due to glutathione synthetase deficiency.

Authors:  R K Pejaver; A H Watson
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

3.  Glutathione synthetase deficiency as a cause of hereditary hemolytic disease.

Authors:  D N Mohler; P W Majerus; V Minnich; C E Hess; M D Garrick
Journal:  N Engl J Med       Date:  1970-12-03       Impact factor: 91.245

4.  Biochemical heterogeneity in glutathione synthetase deficiency.

Authors:  S P Spielberg; M D Garrick; L M Corash; J D Butler; F Tietze; L Rogers; J D Schulman
Journal:  J Clin Invest       Date:  1978-06       Impact factor: 14.808

  4 in total

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