Literature DB >> 7439194

Diagnostic value of orotic acid excretion in heritable disorders of the urea cycle and in hyperammonemia due to organic acidurias.

C Bachmann, J P Colombo.   

Abstract

Orotic acid excretion in urine in increased in ornithine transcarbamylase deficiency, citrullinemia and argininemia; it is barely increased in argininosuccinic aciduria and normal in carbamylphosphate synthetase deficiency and in hyperammonemia due to organic aciduria. The determination of orotic acid excretion is useful in differentiating the cases of hyperammonemia and reduces the need for enzymatic assays on tissue biopsies for decisions on therapy. The data indicate that orotic acid does not merely reflect ammonia concentration in plasma, but depends on carbamylphosphate concentration. Arginine could play a key role in the regulation of ammonia detoxication.

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Year:  1980        PMID: 7439194     DOI: 10.1007/bf01846026

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


  17 in total

1.  Treatment of carbamyl phosphate synthetase deficiency with keto analogues of essential amino acids.

Authors:  M Batshaw; S Brusilow; M Walser
Journal:  N Engl J Med       Date:  1975-05-22       Impact factor: 91.245

2.  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

3.  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

4.  Variants of citrullinaemia.

Authors:  H Wick; C Bachmann; R Baumgartner; T Brechbühler; J P Colombo; U Wiesmann; M J Mihatsch; H Ohnacker
Journal:  Arch Dis Child       Date:  1973-08       Impact factor: 3.791

5.  Enzymatic synthesis of acetylglutamate by mammalian liver preparations and its stimulation by arginine.

Authors:  K Shigesada; M Tatibana
Journal:  Biochem Biophys Res Commun       Date:  1971-09       Impact factor: 3.575

Review 6.  Hereditary metabolic disorders of the urea cycle.

Authors:  B Levin
Journal:  Adv Clin Chem       Date:  1971       Impact factor: 5.394

7.  Propionic acidemia and hyperlysinemia in a case with ornithine transcarbamylase (OTC) deficiency.

Authors:  I Krieger; C Bachmann; W H Gronemeyer; J Cejka
Journal:  J Clin Endocrinol Metab       Date:  1976-10       Impact factor: 5.958

8.  Argininemia.

Authors:  S E Snyderman; C Sansaricq; W J Chen; P M Norton; S V Phansalkar
Journal:  J Pediatr       Date:  1977-04       Impact factor: 4.406

9.  Comparison of plasma creatinine determined with the Greiner Selective Analyser GSA II and the glomerular filtration rate.

Authors:  J P Colombo; E Peheim; W Flury
Journal:  Clin Biochem       Date:  1980-02       Impact factor: 3.281

10.  New pathways of nitrogen excretion in inborn errors of urea synthesis.

Authors:  S W Brusilow; D L Valle; M Batshaw
Journal:  Lancet       Date:  1979-09-01       Impact factor: 79.321

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  18 in total

1.  Astrocytes protect neurons from ammonia toxicity.

Authors:  K V Rama Rao; K S Panickar; A R Jayakumar; M D Norenberg
Journal:  Neurochem Res       Date:  2005-10       Impact factor: 3.996

2.  Biochemical data in ornithine transcarbamylase deficiency (OTCD) carrier risk estimation: logistic discrimination and combination with genetic information.

Authors:  Konrad Oexle
Journal:  J Hum Genet       Date:  2006-02-02       Impact factor: 3.172

3.  DNA analysis of ornithine transcarbamylase deficiency.

Authors:  U Wendel; E Wilichowski; J Schmidtke; C Bachmann
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

4.  Ornithine transcarbamylase variant in a male patient.

Authors:  S Stöckler; F Grossschädl; C Bachmann; A Roscher
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

5.  Carbamyl phosphate synthetase deficiency with lethal neonatal outcome.

Authors:  J Jaeken; H Devlieger; C Bachmann; J Van Aerde; L Corbeel; E Eggermont
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

6.  A new French-Canadian family affected by hyperargininaemia.

Authors:  I A Qureshi; J Letarte; R Ouellet; J Larochelle; B Lemieux
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

7.  Decreased hyperammonaemia and orotic aciduria due to inactivation of ornithine aminotransferase in mice with a hereditary abnormal ornithine carbamoyltransferase.

Authors:  N Seiler; C Grauffel; G Daune-Anglard; S Sarhan; B Knödgen
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

Review 8.  Endogenous ornithine in search for CNS functions and therapeutic applications.

Authors:  N Seiler; G Daune-Anglard
Journal:  Metab Brain Dis       Date:  1993-09       Impact factor: 3.584

9.  Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.

Authors:  B E Kendall; D P Kingsley; J V Leonard; S Lingam; V G Oberholzer
Journal:  J Neurol Neurosurg Psychiatry       Date:  1983-01       Impact factor: 10.154

10.  Chronic mitoinhibition during promotion of hepatocarcinogenesis.

Authors:  E Laconi; P M Rao; S Rajalakshmi; P Pani; D S Sarma
Journal:  Dig Dis Sci       Date:  1991-09       Impact factor: 3.199

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