Literature DB >> 668727

Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia.

W Lehnert, L Schuchmann, R Urbánek, H Niederhoff, N Böhm.   

Abstract

A new case of propionic acidemia is presented, paying special attention to the early symptoms of this disease, such as increased drowsiness, muscular hypotonia, poor feeding, hypothermia, metabolic acidosis, ketonuria and vomiting. Investigation by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS) revealed the excretion of fairly high amounts of 2-methyl-3-oxovaleric acid, a condensation product of two molecules of propionyl-CoA, as well as the known pathological metabolites such as propionic, 3-hydroxypropionic and methylcitric acids. Among the post mortem findings the histological studies of the liver were the most remarkable.

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Year:  1978        PMID: 668727     DOI: 10.1007/BF00444305

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


  11 in total

1.  Localisation of enzymic defect in propionicacidaemia.

Authors:  D Gompertz; C N Storrs; D C Bau; T J Peters; E A Hughes
Journal:  Lancet       Date:  1970-05-30       Impact factor: 79.321

2.  Defective propionate carboxylation in ketotic hyperglycinaemia.

Authors:  Y E Hsia; K J Scully; L E Rosenberg
Journal:  Lancet       Date:  1969-04-12       Impact factor: 79.321

3.  The occurrence of beta-hydroxy-n-valeric acid in a patient with propionic and methylmalonic acidemia.

Authors:  O Stokke; E Jellum; L Eldjarn; R Schnitler
Journal:  Clin Chim Acta       Date:  1973-05-30       Impact factor: 3.786

4.  Isolation and identification of methylcitrate, a major metabolic product of propionate in patients with propionic acidemia.

Authors:  T Ando; K Rasmussen; J M Wright; W L Nyhan
Journal:  J Biol Chem       Date:  1972-04-10       Impact factor: 5.157

5.  Excretion of propionylglycine in propionic acidaemia.

Authors:  K Rasmussen; T Ando; W L Nyhan; D Hull; D Cottom; G Donnell; W Wadlington; A W Kilroy
Journal:  Clin Sci       Date:  1972-06       Impact factor: 6.124

6.  Inherited propionyl-Coa carboxylase deficiency in "ketotic hyperglycinemia".

Authors:  Y E Hsia; K J Scully; L E Rosenberg
Journal:  J Clin Invest       Date:  1971-01       Impact factor: 14.808

7.  Propionicacidemia, a new inborn error of metabolism.

Authors:  F A Hommes; J R Kuipers; J D Elema; J F Jansen; J H Jonxis
Journal:  Pediatr Res       Date:  1968-11       Impact factor: 3.756

8.  Propionic acidemia in patients with ketotic hyperglycinemia.

Authors:  T Ando; K Rasmussen; W L Nyhan; G N Donnell; N D Barnes
Journal:  J Pediatr       Date:  1971-05       Impact factor: 4.406

9.  Idiopathic hyperglycinemia: isolation and identification of three previously undescribed urinary ketones.

Authors:  J H Menkes
Journal:  J Pediatr       Date:  1966-09       Impact factor: 4.406

10.  3-hydroxypropionate: significance of -oxidation of propionate in patients with propionic acidemia and methylmalonic acidemia.

Authors:  T Ando; K Rasmussen; W L Nyhan; D Hull
Journal:  Proc Natl Acad Sci U S A       Date:  1972-10       Impact factor: 11.205

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  8 in total

1.  Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two cases.

Authors:  A Kohlschütter; H P Willig; D Schlamp; K Kruse; E R McCabe; H J Schäfer; G Beckenkamp; R Rohkamm
Journal:  Eur J Pediatr       Date:  1987-11       Impact factor: 3.183

2.  4-hydroxyisovaleric acid: a new metabolite in isovaleric acidemia.

Authors:  W Lehnert; H Niederhoff
Journal:  Eur J Pediatr       Date:  1981-07       Impact factor: 3.183

3.  3-Methylglutaconic and 3-methylglutaric aciduria in a patient with suspected 3-methylglutaconyl-CoA hydratase deficiency.

Authors:  W Lehnert; J Scharf; U Wendel
Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

4.  Seven years of experience with selective screening for organic acidurias.

Authors:  W Lehnert; H Niederhoff
Journal:  Eur J Pediatr       Date:  1984-08       Impact factor: 3.183

5.  A case of biotin-responsive 3-methylcrotonylglycin- and 3-hydroxyisovaleric aciduria.

Authors:  W Lehnert; H Niederhoff; A Junker; H Saule; W Frasch
Journal:  Eur J Pediatr       Date:  1979-10       Impact factor: 3.183

6.  Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings.

Authors:  W Lehnert; U Wendel; S Lindenmaier; N Böhm
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

7.  A familial progressive neurodegenerative disease with 2-oxoglutaric aciduria.

Authors:  A Kohlschütter; A Behbehani; U Langenbeck; M Albani; P Heidemann; G Hoffmann; J Kleineke; W Lehnert; U Wendel
Journal:  Eur J Pediatr       Date:  1982-02       Impact factor: 3.183

8.  Long-term results of selective screening for inborn errors of metabolism.

Authors:  W Lehnert
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

  8 in total

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