Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
|
pubmed:dateCreated |
1991-11-14
|
pubmed:abstractText |
A newborn infant suffered from severe omphalitis resistant to antibiotic therapy. The combination of the symptoms: delayed separation of the umbilical cord, omphalitis, impairment of wound-healing and extreme leukocytosis led to the diagnosis of LFA-1 (leukocyte function antigen)-deficiency, which was confirmed by monoclonal antibodies. The pathophysiology of this disorder is described shortly.
|
pubmed:language |
ger
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0026-9298
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
139
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
418-20
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:1922120-Anti-Bacterial Agents,
pubmed-meshheading:1922120-Bacterial Infections,
pubmed-meshheading:1922120-Drug Therapy, Combination,
pubmed-meshheading:1922120-Granulocytes,
pubmed-meshheading:1922120-Humans,
pubmed-meshheading:1922120-Immunologic Deficiency Syndromes,
pubmed-meshheading:1922120-Infant, Newborn,
pubmed-meshheading:1922120-Lymphocyte Function-Associated Antigen-1,
pubmed-meshheading:1922120-Umbilicus
|
pubmed:year |
1991
|
pubmed:articleTitle |
[LFA-1 defect: a rare granulocyte function disorders as a cause of therapy-resistant omphalitis in newborn infants].
|
pubmed:affiliation |
Pädiatrische Abteilung, Altonaer Kinderkrankenhaus, Hamburg.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
|