Rhabdomyolysis caused by an inherited metabolic disease: Very long-chain Acyl-CoA dehydrogenase deficiency [1]

American Journal of Medicine

Volumn 119, Issue 2, 2006, Pages 176-179

  Voermans, Nicol C ^a   Van Engelen, Baziel G ^a   Kluijtmans, Leo A ^a   Stikkelbroeck, Nike M ^a   Hermus, Ad R ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE PALMITOYLTRANSFERASE; LONG CHAIN ACYL COENZYME A DEHYDROGENASE; OLEIC ACID; PALMITIC ACID; VERY LONG CHAIN FATTY ACID;

ADULT; ANAMNESIS; CASE REPORT; CHEMICAL ANALYSIS; CLINICAL FEATURE; DIAGNOSTIC PROCEDURE; DIET THERAPY; ELECTROCARDIOGRAPHY; ENZYME DEFICIENCY; EXERCISE; HUMAN; LETTER; LIFESTYLE; MALE; METABOLIC DISORDER; MITOCHONDRIAL RESPIRATION; MYOGLOBINURIA; PHYSICAL EXAMINATION; PRIORITY JOURNAL; PROPHYLAXIS; RECURRENT DISEASE; RHABDOMYOLYSIS; URINALYSIS;

ACYL-COA DEHYDROGENASE, LONG-CHAIN; ADULT; EXERTION; HUMANS; LIPID METABOLISM, INBORN ERRORS; MALE; MITOCHONDRIAL DISEASES; RHABDOMYOLYSIS;

EID: 31444447465     PISSN: 00029343     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjmed.2005.07.064     Document Type: Letter

References (9)

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