Literature DB >> 2943344

Mass spectrometric identification of 2-hydroxy-sebacic acid in the urines of patients with neonatal adrenoleukodystrophy and Zellweger syndrome.

F Rocchiccioli, P H Cartier, P Aubourg, P F Bougnères.   

Abstract

The urines of children with neonatal adrenoleukodystrophy and Zellweger syndrome contained an excess of unusual even- and odd-numbered dicarboxylic acids with a chain length of from 5 to 15 carbon atoms, as well as 2-hydroxy-compounds, including 2-hydroxy-isocaproate, 2-hydroxy-glutarate and 2-hydroxy-sebacate. The latter product, not previously found in metabolic diseases, appears as an additional useful marker of these peroxisomal disorders.

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Year:  1986        PMID: 2943344     DOI: 10.1002/bms.1200130609

Source DB:  PubMed          Journal:  Biomed Environ Mass Spectrom        ISSN: 0887-6134


  3 in total

1.  Characteristic urine organic acid profile in peroxisomal biogenesis disorders.

Authors:  S H Korman; H Mandel; A Gutman
Journal:  J Inherit Metab Dis       Date:  2000-06       Impact factor: 4.982

2.  Stereoselective analysis of 2-hydroxysebacic acid in urine of patients with Zellweger syndrome and of premature infants fed with medium-chain triglycerides.

Authors:  A Muth; A Mosandl; R J A Wanders; M J M Nowaczyk; I Baric; H Böhles; A C Sewell
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

3.  The metabolic analysis of psoriasis identifies the associated metabolites while providing computational models for the monitoring of the disease.

Authors:  Aigar Ottas; Dmytro Fishman; Tiia-Linda Okas; Külli Kingo; Ursel Soomets
Journal:  Arch Dermatol Res       Date:  2017-07-10       Impact factor: 3.017

  3 in total

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