Acute, severe cardiomyopathy as main symptom of late-onset very long- chain acyl-coenzyme A dehydrogenase deficiency

European Journal of Pediatrics

Volumn 157, Issue 12, 1998, Pages 992-995

  Parini, R ^f   Menni, F ^f   Garavaglia, B ^a   Fesslova, V ^b   Melotti, D ^c   Massone, M L ^d   Lamantea, E ^a   Rimoldi, M ^a   Vizziello, P ^e   Gatti, R ^d  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

^b Sezione di Cardiologia Pediatrica   (Italy)

^c Lab Biochim Sezione Malat M   (Italy)

^d G GASLINI INSTITUTE   (Italy)

^e Serv Igiene Mentale Eta Evolutiva   (Italy)

^f Clinica Pediatrica II   (Italy)

Author keywords

oxidation; Cardiomyopathy; Myoglobinuria; Myopathy; VLCAD deficiency

Indexed keywords

ACYL COENZYME A DEHYDROGENASE; CARNITINE; FATTY ACID;

ACUTE DISEASE; ARTICLE; CARDIOMYOPATHY; CASE REPORT; DISEASE COURSE; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FIBROBLAST; GLUCOSE BLOOD LEVEL; HUMAN; MALE; MYOGLOBINURIA; MYOPATHY; PRESCHOOL CHILD; PRIORITY JOURNAL; SYMPTOM;

ACUTE DISEASE; ACYL-COA DEHYDROGENASE; ACYL-COA DEHYDROGENASE, LONG-CHAIN; AGE OF ONSET; CARDIOMYOPATHIES; CHILD, PRESCHOOL; DIARRHEA; HUMANS; MALE;

EID: 15144355032     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310050984     Document Type: Article

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