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PMID: 2326302 Published · ppublish English Clinical Trial Comparative Study Controlled Clinical Trial Journal Article

Diagnosis of medium chain acyl-CoA dehydrogenase deficiency by stable isotope dilution analysis of urinary acylglycines: retrospective and prospective studies, and comparison of its accuracy to acylcarnitine identification by FAB/mass spectrometry.

Progress in clinical and biological research ·Vol. 321 ·1990-00-00 ·Pages 411-8

Rinaldo P, O'Shea JJ, Welch RD, Tanaka K

Abstract

In summary, we have demonstrated that the accurate quantitation of urinary HG and PPG by stable isotope dilution analysis is currently the most reliable method for the diagnosis of MCAD deficiency. This method is particularly useful for testing random samples from asymptomatic patients without any provocative test, and it is suitable to widely survey a fairly large population, such as patients with episodic manifestations and families with a history of SIDS.

MeSH Terms
Acyl-CoA Dehydrogenase Acyl-CoA Dehydrogenases/deficiency Carbon Isotopes Electrons Fatty Acids/urine Glycine/urine Humans Mass Spectrometry Nitrogen Isotopes Prospective Studies Retrospective Studies Sudden Infant Death/epidemiology
Chemicals
Carbon Isotopes Fatty Acids Nitrogen Isotopes Acyl-CoA Dehydrogenases Acyl-CoA Dehydrogenase Glycine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rinaldo P
Yale University School of Medicine, Department of Human Genetics, New Haven, CT 06510.
O'Shea J J
Welch R D
Tanaka K
Article Info
Journal
Progress in clinical and biological research
Abbr.
Prog Clin Biol Res
ISSN
0361-7742
Published
1990-00-00
Pages
411-8
Language
English
Region
United States
NLM ID
7605701
Subset
IM
External Links
PubMed source
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