Literature DB >> 668733

Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiency.

C van der Heiden, H D Bakker, J Desplanque, M Brink, P K de Bree, S K Wadman.   

Abstract

Dietary treatment of a male patient suffering from the delayed-onset type of OCT deficiency was attempted. Control of the hyperammonemia was attempted by restriction of protein intake, guided by monitoring the plasma ammonia and regular checking of the serum amino acid levels. The influence of supplementary citric acid or lactulose therapy on the plasma ammonia level was investigated and found to be negligible. The therapeutic effect of supplying ornithine and arginine (an essential amino acid in urea cycle disorders) is described. Despite intensive dietary treatment over two and a half years, a incorrigible hyperammonemic crisis resulted in the sudden death of our patient.

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Year:  1978        PMID: 668733     DOI: 10.1007/BF00445611

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  38 in total

1.  [Direct determination of ammonium in blood and tissue extracts by means of the phenol by chlorite reaction].

Authors:  K KONITZER; S VOIGT
Journal:  Clin Chim Acta       Date:  1963-01       Impact factor: 3.786

2.  Hyperammonaemia due to ornithine transcarbamylase deficiency.

Authors:  I J Hopkins; J F Connelly; A G Dawson; F J Hird; T G Maddison
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

3.  Biochemical investigations of hyperammonaemia.

Authors:  B Levin; V G Oberholzer; L Sinclair
Journal:  Lancet       Date:  1969-07-26       Impact factor: 79.321

4.  Urinary excretion of 3 -methylxanthine and related compounds in children.

Authors:  A H van Gennip; P K de Bree; C van der Heiden; S K Wadman; J Haverkamp; J F Vliegenthart
Journal:  Clin Chim Acta       Date:  1973-04-30       Impact factor: 3.786

5.  Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency.

Authors:  E M Short; H O Conn; P J Snodgrass; A G Campbell; L E Rosenberg
Journal:  N Engl J Med       Date:  1973-01-04       Impact factor: 91.245

6.  Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.

Authors:  P Sunshine; J E Lindenbaum; H L Levy; J M Freeman
Journal:  Pediatrics       Date:  1972-07       Impact factor: 7.124

7.  Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.

Authors:  B Levin; J M Abraham; V G Oberholzer; E A Burgess
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

8.  Rapid, high-resolution, two-dimensional amino acid chromatography on micro scale chromatograms.

Authors:  S K Wadman; H F de Jonge; P K de Bree
Journal:  Clin Chim Acta       Date:  1969-07       Impact factor: 3.786

9.  Arginosuccinicaciduria. The hair abnormality.

Authors:  J L Potter; G D Timmons; R West; A A Silvidi
Journal:  Am J Dis Child       Date:  1974-05

10.  [Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)].

Authors:  M A Beaudry; J Letarte; R Collu; G Leboeuf; J R Ducharme; S B Melancon; L Dallairf
Journal:  Diabete Metab       Date:  1975-03
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  4 in total

1.  Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.

Authors:  Renata C Gallagher; Christina Lam; Derek Wong; Stephen Cederbaum; Ronald J Sokol
Journal:  J Pediatr       Date:  2014-01-30       Impact factor: 4.406

2.  Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment.

Authors:  C vd Heiden; M Brink; P K de Bree; F J v Sprang; S K Wadman; J M de Pater; J P van Biervliet
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

3.  Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentration.

Authors:  U Wendel; J Wieland; H J Bremer; C Bachmann
Journal:  Eur J Pediatr       Date:  1989-01       Impact factor: 3.183

4.  Late onset ornithine carbamoyl transferase deficiency in males.

Authors:  E Drogari; J V Leonard
Journal:  Arch Dis Child       Date:  1988-11       Impact factor: 3.791

  4 in total

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