Literature DB >> 947635

Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria.

N Gregersen, R Lauritzen, K Rasmussen.   

Abstract

Suberylglycine (HOOC(CH2)6CONHCH2COOH) was found in the urine from a patient with C6-C10-omega-dicarboxylic aciduria and unexplained episodes of lethargy and unconsciousness. The total excretion of adipic, suberic and sebacic acid ranged from 0.77 to 1.3 mg/mg creatinine after episodes of acute attack of the disease. Suberylglycine, identified by gas chromatography/mass spectrometry, was repeatedly found in the urine samples. The amount of this conjugate ranged from 0.2 to 0.5 mg/mg creatinine. The precursors of the dicarboxylic acids are suggested to be long chain monocarboxylic acids, oxidized through omega- and beta-oxidation to adipic, suberic and sebacic acid. Suberylglycine is subsequently formed by glycine-N-acylase catalyzed conjugation.

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Year:  1976        PMID: 947635     DOI: 10.1016/0009-8981(76)90355-7

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  27 in total

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Journal:  J Inherit Metab Dis       Date:  2000-05       Impact factor: 4.982

2.  N-Dicarboxylmonoglycines: excretion in dicarboxylic acidurias and mode of formation.

Authors:  I H Grøn; N Gregersen; K Rasmussen
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

Review 3.  The clinical manifestation of MCAD deficiency: challenges towards adulthood in the screened population.

Authors:  Ulrich A Schatz; Regina Ensenauer
Journal:  J Inherit Metab Dis       Date:  2010-06-08       Impact factor: 4.982

4.  Evaluation of diagnostic fasting in the investigation of hypoglycemia in children omani experienc.

Authors:  Bhasker Bappal; Waad-Allah Mula-Abed
Journal:  Oman Med J       Date:  2007-10

5.  A new patient with dicarboxylic aciduria suggestive of medium-chain Acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome.

Authors:  J A Del Valle; M J Garcia; B Merinero; C Pérez-Cerdá; F Roman; A Jimenez; M Ugarte; M Martínez-Pardo; C Ludeña; C Camarero
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

6.  The differential diagnosis of dicarboxylic aciduria.

Authors:  M Duran; J B De Klerk; S K Wadman; L Bruinvis; D Ketting
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

7.  The microsomal dicarboxylyl-CoA synthetase.

Authors:  J Vamecq; E de Hoffmann; F Van Hoof
Journal:  Biochem J       Date:  1985-09-15       Impact factor: 3.857

8.  A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD).

Authors:  B S Andresen; P Bross; T G Jensen; V Winter; I Knudsen; S Kølvraa; U B Jensen; L Bolund; M Duran; J J Kim
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

9.  Gas chromatography--mass spectrometry (GC--MS) diagnosis of two cases of medium chain acyl-CoA dehydrogenase deficiency.

Authors:  P Divry; C Vianey-Liaud; J Cotte
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

10.  Fatty acyl-CoA dehydrogenase deficiency: enzyme measurement and studies on alternative metabolism.

Authors:  N Gregersen
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

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