Literature DB >> 556398

Protein load in argininosuccinic aciduria: thoughts on its biochemical implications.

H Böhles, D Harms, H Heid, F C Sitzmann, W Fekl.   

Abstract

A patient with argininosuccinc aciduria was charged with 50 grams of protein, which was followed by considerable hyperammonemia. There was no response in further urea formation; but there was a considerable production of orotic acid, a precursor of pyrimidines. This makes orotic acid to an important diagnostic tool for the diagnosis of impaired urea formation. The patient's plasma amino acid pattern led to the suggestion that orotic acid synthesis is initiated by increased de novo formation of carbamyl phosphate in the cytosol and not by deviation of already existing intramitochondrial carbamyl phosphate.

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Year:  1978        PMID: 556398     DOI: 10.1007/bf02021112

Source DB:  PubMed          Journal:  Z Ernahrungswiss        ISSN: 0044-264X


  13 in total

1.  Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.

Authors:  N A CARSON; D W NEILL
Journal:  Arch Dis Child       Date:  1962-10       Impact factor: 3.791

2.  A FAMILY AFFECTED BY ARGININO-SUCCINIC ACIDURIA.

Authors:  K WALLIS; S BEER; J FISCHL
Journal:  Helv Paediatr Acta       Date:  1963-11

3.  Argininosuccinic aciduria: identification and reactions of the abnormal metabolite in a newly described form of mental disease, with some preliminary metabolic studies.

Authors:  R G WESTALL
Journal:  Biochem J       Date:  1960-10       Impact factor: 3.857

Review 4.  Two carbamyl phosphate synthetases of mammals: specific roles in control of pyrimidine and urea biosynthesis.

Authors:  M Tatibana; K Shigesada
Journal:  Adv Enzyme Regul       Date:  1972

5.  Effect of low, normal and high dietary protein intake on urinary amino acid excretion and plasma aminogram in children.

Authors:  G Holmgren
Journal:  Nutr Metab       Date:  1974       Impact factor: 4.169

6.  Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency.

Authors:  A S Goldstein; N J Hoogenraad; J D Johnson; K Fukanaga; E Swierczewski; H M Cann; P Sunshine
Journal:  Pediatr Res       Date:  1974-01       Impact factor: 3.756

7.  Metabolism of compounds labeled with 15 N by an infant with congenital hyperammonemia.

Authors:  J F Nicholson; J M Freeman
Journal:  Pediatr Res       Date:  1972-04       Impact factor: 3.756

8.  The therapy of hyperammonemia due to ornithine transcarbamylase defiency in a male neonate.

Authors:  S E Snyderman; C Sansaricq; S V Phansalkar; R C Schacht; P M Norton
Journal:  Pediatrics       Date:  1975-07       Impact factor: 7.124

9.  Mechanisms for the formation of alanine and aspartate on rat liver in vivo after administration of ammonium chloride.

Authors:  J T Brosnan; D H Williamson
Journal:  Biochem J       Date:  1974-03       Impact factor: 3.857

10.  Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes.

Authors:  J C Haworth; T L Perry; J P Blass; S Hansen; N Urquhart
Journal:  Pediatrics       Date:  1976-10       Impact factor: 7.124

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  1 in total

1.  Argininosuccinic aciduria: metabolic studies and effects of treatment with keto-analogues of essential amino acids.

Authors:  H Böhles; H Heid; D Harms; D Schmid; W Fekl
Journal:  Eur J Pediatr       Date:  1978-07-19       Impact factor: 3.183

  1 in total

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