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1.
J Pediatr ; 88(2): 229-35, 1976 Feb.
Article in English | MEDLINE | ID: mdl-1249684

ABSTRACT

A patient is described in whom lactic acidosis of very severe degree was found to coincide with the presence of beta-methylcrotonic acid and rho-hydroxyphenyllactic acid in urine in large amounts, while beta-hydroxyisovaleric acid was found to be a relatively minor excretion product. Beta-methylcrotonic acid is demonstrated, for the first time, to be present in blood and CSF. These findings are discussed in relation to the patients previously reported to have beta-methylcrotonylglycinuria and raise the possibility that our patient's organic aciduria may be secondary to acquired disease rather than to an inborn error of metabolism.


Subject(s)
Butyrates/urine , Crotonates/urine , Lactates/urine , Metabolic Diseases/urine , Amino Acids/blood , Amino Acids/urine , Carboxylic Acids/blood , Carboxylic Acids/cerebrospinal fluid , Humans , Hydroxy Acids/urine , Infant, Newborn , Metabolic Diseases/blood , Metabolic Diseases/cerebrospinal fluid , Phenols/urine , Valerates/urine
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