Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiency

Journal of Inherited Metabolic Disease

Volumn 20, Issue 6, 1997, Pages 842-843

  Mayatepek, E ^a   Koch, H G ^b   Hoffmann, G F ^c  

^a UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

^b UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^c University Children's Hospital   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DICARBOXYLIC ACID; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE;

ARTICLE; CASE REPORT; ENZYME DEFICIENCY; FATTY ACID METABOLISM; FEMALE; HUMAN; HYPERURICEMIA; HYPOGLYCEMIA; PRESCHOOL CHILD; PROGNOSIS; SYMPTOM;

ACYL-COA DEHYDROGENASE; ACYL-COA DEHYDROGENASES; BLOOD GLUCOSE; BRAIN EDEMA; FEMALE; HUMANS; HYPOGLYCEMIA; HYPOXANTHINE; INFANT; SEIZURES; URIC ACID;

EID: 0030777849     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005300708445     Document Type: Article

References (2)

1. Davidson-Mundt A, Luder AS, Greene CL (1992) Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiency. J Pediatr 120: 444-446.
2. Treem WR, Witzleben CA, Piccoli DA et al (1986) Medium-chain and long-chain acyl-CoA dehydrogenase deficiency: clinical, pathologic, and ultrastructural differentiation from Reye's syndrome. Hepatology 6: 1270-1278.