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Biochemical studies in a patient with defects in the metabolism of acyl‐CoA and sarcosine: Another possible case of glutaric aciduria type II
Author(s) -
Gregersen N.,
Kølvraa S.,
Rasmussen K.,
Christensen E.,
Brandt N. J.,
Ebbesen F.,
Hansen F. H.
Publication year - 1980
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf02312527
Subject(s) - glutaric acid , excretion , isobutyric acid , caproic acid , chemistry , sarcosine , metabolism , catabolism , butyric acid , endocrinology , medicine , biochemistry , amino acid , glycine , organic chemistry
The clinical and biochemical abnormalities in a neonate, who died in coma accompanied by severe hypoglycaemia at the age of 3 days, are described. The study of the urinary metabolic profiles of organic acids and amino acids revealed that the excretion rates of glutaric acid, isovaleric acid, isovalerylglycine, 3‐hydroxyisovaleric acid and isobutyric acid were very high. Increased excretion rates were also found for 2‐methylbutyric acid, adipic acid, caproylglycine, 5‐hydroxycaproic acid, caproic acid and butyric acid. The amino acid, sarcosine, was excreted in enhanced amounts and the patient had lactic aciduria, whereas the excretion of 3‐hydroxybutyric acid was only moderately increased. This abnormal excretion pattern is consistent with a defect in the metabolism of acyl‐CoAs and sarcosine. Normal activity of glutaryl‐CoA dehydrogenase was found, excluding glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria type I).