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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1986-7-25
|
| pubmed:abstractText |
Lipoprotein-lipase deficiency is an uncommon disease, inherited as an autosomal recessive pattern. The authors report two cases: the first one is a fourteen years old girl. It is revealed by abdominal pain; the diagnosis is detected by a milky plasma and confirmed by the enzyme activity which is dramatically decreased; the other one is a seven year old boy, who shows several pancreatitis but in whom the enzyme activity is not so low, perhaps because of genotypical difference.
|
| pubmed:language |
fre
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0031-4021
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
41
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
33-9
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:3725507-Acute Disease,
pubmed-meshheading:3725507-Adolescent,
pubmed-meshheading:3725507-Child,
pubmed-meshheading:3725507-Female,
pubmed-meshheading:3725507-Humans,
pubmed-meshheading:3725507-Hyperlipoproteinemia Type I,
pubmed-meshheading:3725507-Hyperlipoproteinemias,
pubmed-meshheading:3725507-Pancreatitis,
pubmed-meshheading:3725507-Time Factors
|
| pubmed:articleTitle |
[Lipoprotein lipase deficiency. Apropos of 2 cases].
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|