Rhabdomyolysis in early-onset very long-chain acyl-CoA dehydrogenase deficiency despite normal glucose after fasting

Journal of Inherited Metabolic Disease

Volumn 28, Issue 6, 2005, Pages 1151-1152

  Engbers, Hannelie M ^a   Dorland, L ^a   De Sain, M G M ^a   Eskes, P F ^b   Visser, G ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b MEANDER MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ACYLCARNITINE; CARNITINE; CREATINE KINASE; GLUCOSE; LONG CHAIN ACYL COENZYME A DEHYDROGENASE;

ARTICLE; CASE REPORT; DIAGNOSTIC IMAGING; DIET RESTRICTION; ENZYME DEFICIENCY; GLUCOSE BLOOD LEVEL; HUMAN; HYPOGLYCEMIA; LABORATORY TEST; MALE; NEWBORN; NEWBORN PERIOD; ONSET AGE; RHABDOMYOLYSIS;

ACYL-COA DEHYDROGENASE, LONG-CHAIN; BLOOD GLUCOSE; CARNITINE; FASTING; GLUCOSE; HUMANS; HYPOGLYCEMIA; INFANT; METABOLISM, INBORN ERRORS; RHABDOMYOLYSIS;

EID: 31644449017     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-005-0190-y     Document Type: Article

References (2)

1. Roe CR, Sweetman L, Roe DS, et al (2002) Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride. J Clin Invest 110: 259-269.
2. Vianey-Saban C, Divry P, Brivet M, et al (1998) Mitochondrial very long-chain acyl-CoA dehydrogenase deficiency: Clinical characteristics and diagnostic considerations in 30 patients. Clin Chim Acta 269: 43-62.