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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
12
|
| pubmed:dateCreated |
1999-3-4
|
| pubmed:abstractText |
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.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Dec
|
| pubmed:issn |
0340-6199
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
157
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
992-5
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:9877038-Acute Disease,
pubmed-meshheading:9877038-Acyl-CoA Dehydrogenase,
pubmed-meshheading:9877038-Acyl-CoA Dehydrogenase, Long-Chain,
pubmed-meshheading:9877038-Age of Onset,
pubmed-meshheading:9877038-Cardiomyopathies,
pubmed-meshheading:9877038-Child, Preschool,
pubmed-meshheading:9877038-Diarrhea,
pubmed-meshheading:9877038-Humans,
pubmed-meshheading:9877038-Male
|
| pubmed:year |
1998
|
| pubmed:articleTitle |
Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiency.
|
| pubmed:affiliation |
Clinica Pediatrica II, Istituti Clinici di Perfezionamento, Milano, Italy. Rossella.Parini@unimi.it
|
| pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|