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J Pediatr ; 90(5): 746-50, 1977 May.
Article de Anglais | MEDLINE | ID: mdl-856963

RÉSUMÉ

Biochemical and morphologic studies on a patient with glutaric aciduria are presented. Generalized aminoaciduria, alpha-aminoadipic aciduria, and saccharopinuria were noted just prior to death, as well as glutaconic aciduria greater than beta-hydroxyglutaric aciduria. Mutant liver mitochondria did not oxidize glutaryl-CoA to glutaconyl-CoA, indicating deficiency of glytaryl-CoA dehydrogenase. Autopsy revealed cerebral edema, ischemic neuronal changes, and striatal degeneration in the brain with fatty changes in liver, kidney, and myocardium.


Sujet(s)
Aminoacidopathies congénitales/anatomopathologie , Glutarates/urine , Oxidoreductases/déficit , Aminoacidopathies congénitales/urine , Autopsie , Encéphale/anatomopathologie , Chimie du cerveau , Enfant , Glutarates/analyse , Humains , Hydroxylysine/métabolisme , Nourrisson , Rein/anatomopathologie , Foie/anatomopathologie , Lysine/métabolisme , Mâle , Mitochondries du foie/métabolisme , Myocarde/anatomopathologie , Tryptophane/métabolisme
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