Creatine kinase and uric acid: Early warning for metabolic imbalance resulting from disorders of fatty acid oxidation

European Journal of Pediatrics

Volumn 160, Issue 10, 2001, Pages 599-602

  Marsden, Deborah ^a   Nyhan, William L ^b   Barshop, Bruce A ^b  

^a HARVARD UNIVERSITY   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Creatine phosphokinase; Disorders of fatty acid oxidation; Uric acid

Indexed keywords

CEFOTAXIME; CREATINE KINASE; GLUCOSE; LONG CHAIN ACYL COENZYME A DEHYDROGENASE; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE; OXIDOREDUCTASE; UNCLASSIFIED DRUG; URIC ACID; VERY LONG CHAIN ACYL COENZYME A DEHYDROGENASE;

ADOLESCENT; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; DEHYDRATION; DIARRHEA; DISEASE COURSE; DNA DETERMINATION; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FEMALE; FEVER; GLUCOSE BLOOD LEVEL; HUMAN; HYPOGLYCEMIA; HYPOPITUITARISM; INFANT; LETHARGY; LONG CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY; MALE; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY; METABOLIC DISORDER; MUTATION; PARENTERAL NUTRITION; PRIORITY JOURNAL; RHABDOMYOLYSIS; URINALYSIS; VERY LONG CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY; VOMITING;

3-HYDROXYACYL COA DEHYDROGENASES; ACYL-COA DEHYDROGENASE; ACYL-COA DEHYDROGENASE, LONG-CHAIN; ADOLESCENT; BIOLOGICAL MARKERS; CHILD; CHILD, PRESCHOOL; CREATINE KINASE; FEMALE; HUMANS; INFANT; MALE; OXIDATION-REDUCTION; URIC ACID;

EID: 0034786382     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310100808     Document Type: Article

References (10)

1. Hyperuricemia in medium-chain acyl-coenzyme dehydrogenase deficiency
2. Taylor's story (MCAD) FOD
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5. Identification of a common mutation in patients with medium-chain acyl-CoA dehydration deficiency
6. Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiency
7. Hyperuricemia as the main symptom of medium-chain acyl-CoA dehydrogenase deficiency
8. Case report: Neonatal medium-chain acyl-CoA dehydrogenase deficiency presenting with very high creatine kinase levels
9. Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency