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Pre- and postnatal diagnosis of peroxisomal disorders using stable-isotope dilution gas chromatography - mass spectrometry

Authors :
Verhoeven, N. M.
Kulik, W.
van den Heuvel, C. M. M.
Jakobs, C.
Source :
Journal of Inherited Metabolic Disease; January 1995, Vol. 18 Issue: Supplement 1 p45-60, 16p
Publication Year :
1995

Abstract

Summary Quantitative analysis of the following peroxisomal metabolites is reported: very long-chain fatty acids (VLCFA), pipecolic acid, bile acid intermediates, phytanic and pristanic acid, in plasma, urine, cerebrospinal fluid (CSF), blood spots collected at neonatal screening and amniotic fluid. An overview is given of the concentrations of these metabolites in body fluids from control subjects and all patients investigated so far in this laboratory. The method of choice is gas chromatography — mass spectrometry (GC-MS) with electron capture detection, combined with the use of stable-isotope-labelled internal standards

Details

Language :
English
ISSN :
01418955 and 15732665
Volume :
18
Issue :
Supplement 1
Database :
Supplemental Index
Journal :
Journal of Inherited Metabolic Disease
Publication Type :
Periodical
Accession number :
ejs15320058
Full Text :
https://doi.org/10.1007/BF00711428