Literature DB >> 10771848

Arginase deficiency.

R Christopher1, V Rajivnath, K T Shetty.   

Abstract

Hyperargininemia due to arginase deficiency is a rare, inherited, urea cycle disorder. We report a case of arginase deficiency in a 5-year old boy presenting with mild hyperammonemia, hyperargininemia, and dibasic aminoaciduria.

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Mesh：

Year:  1997        PMID： 10771848     DOI： 10.1007/bf02752462

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


  3 in total

1.  The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23.

Authors:  R S Sparkes; G J Dizikes; I Klisak; W W Grody; T Mohandas; C Heinzmann; S Zollman; A J Lusis; S D Cederbaum
Journal:  Am J Hum Genet       Date:  1986-08       Impact factor: 11.025

2.  Hyperargininemia with arginase deficiency.

Authors:  S D Cederbaum; K N Shaw; E B Spector; M A Verity; P J Snodgrass; G I Sugarman
Journal:  Pediatr Res       Date:  1979-07       Impact factor: 3.756

3.  Induction of arginase activity with the Shope papilloma virus in tissue culture cells from an argininemic patient.

Authors:  S Rogers; A Lowenthal; H G Terheggen; J P Columbo
Journal:  J Exp Med       Date:  1973-04-01       Impact factor: 14.307
  3 in total
  2 in total

1.  Autistic-like findings associated with a urea cycle disorder in a 4-year-old girl.

Authors:  Işik Görker; Umran Tüzün
Journal:  J Psychiatry Neurosci       Date:  2005-03       Impact factor: 6.186

2.  Hyperargininemia Experiences over Last 7 Years from a Tertiary Care Center.

Authors:  Sadanandavalli Retnaswami Chandra; Rita Christopher; Chakravarthula Nitin Ramanujam; Ganaraja Valakunja Harikrishna
Journal:  J Pediatr Neurosci       Date:  2019 Jan-Mar
  2 in total

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