Literature DB >> 2707281

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

U Wendel1, J Wieland, H J Bremer, C Bachmann.   

Abstract

In a male with a partial defect of ornithine transcarbamylase (OTC) we observed that maintenance of arginine supply was crucial for adequate metabolic control in conjunction with a low protein diet. The arginine supplement had to be given such that the concentrations of arginine and ornithine in plasma were above 50 mumol/l. It appears that arginine is needed not only as an essential amino acid for protein synthesis but also as a precursor of ornithine. In this patient the substitution thus aimed at increasing the intramitochondrial ornithine in order to reach a critical substrate concentration for the kinetically abnormal OTC.

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Year:  1989        PMID: 2707281     DOI: 10.1007/BF00444132

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


  18 in total

1.  Hereditary ornithine transcarbamylase deficiency. Report of two male cases with residual enzymatic activity.

Authors:  J M Saudubray; L Cathelineau; J M Laugier; C Charpentier; J A Lejeune; P Mozziconacci
Journal:  Acta Paediatr Scand       Date:  1975-05

2.  Some kinetic properites of liver ornithine carbamoyl transferase (OCT) in a patient with OCT deficiency.

Authors:  C van der Heiden; J Desplanque; H D Bakker
Journal:  Clin Chim Acta       Date:  1977-11-01       Impact factor: 3.786

3.  Endogenous renal transport of free amino acids in infancy and childhood.

Authors:  J Brodehl; K Gellissen
Journal:  Pediatrics       Date:  1968-09       Impact factor: 7.124

4.  Chronic benzoate therapy in a boy with partial ornithine transcarbamylase deficiency.

Authors:  J Letarte; I A Qureshi; R Ouellet; M Godard
Journal:  J Pediatr       Date:  1985-05       Impact factor: 4.406

5.  Immunochemical assay in 16 boys with ornithine transcarbamylase deficiency.

Authors:  B Francois; P Briand; L Cathelineau
Journal:  Adv Exp Med Biol       Date:  1982       Impact factor: 2.622

6.  Determination of orotic acid in children's urine.

Authors:  C Bachmann; J P Colombo
Journal:  J Clin Chem Clin Biochem       Date:  1980-05

7.  Study of enzyme defect in a case of ornithine transcarbamylase deficiency.

Authors:  I A Qureshi; J Letarte; R Quellet
Journal:  Diabete Metab       Date:  1978-12

8.  Arginine-responsive asymptomatic hyperammonemia in the premature infant.

Authors:  M L Batshaw; R C Wachtel; G H Thomas; A Starrett; S W Brusilow
Journal:  J Pediatr       Date:  1984-07       Impact factor: 4.406

9.  Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.

Authors:  S W Brusilow
Journal:  J Clin Invest       Date:  1984-12       Impact factor: 14.808

10.  Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant.

Authors:  P MacLeod; S Mackenzie; C R Scriver
Journal:  Can Med Assoc J       Date:  1972-09-09       Impact factor: 8.262

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  2 in total

Review 1.  Diagnosis and management of inborn errors of metabolism.

Authors:  J E Wraith
Journal:  Arch Dis Child       Date:  1989-10       Impact factor: 3.791

2.  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 in total

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