Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiency.
Eur J Pediatr
; 157(12): 992-5, 1998 Dec.
Article
em En
| MEDLINE
| ID: mdl-9877038
UNLABELLED: A 5-year-old boy with late-onset very long-chain acyl-CoA-dehydrogenase (VLCAD) deficiency presented with acute cardiomyopathy, myopathy, gross myoglobinuria and normoglycaemia. The clinical course after diagnosis was favourable. CONCLUSION: late-onset VLCAD deficiency may present as acute cardiomyopathy.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Acil-CoA Desidrogenase de Cadeia Longa
/
Cardiomiopatias
Tipo de estudo:
Diagnostic_studies
Limite:
Child, preschool
/
Humans
/
Male
Idioma:
En
Revista:
Eur J Pediatr
Ano de publicação:
1998
Tipo de documento:
Article
País de afiliação:
Itália
País de publicação:
Alemanha