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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6-7
|
pubmed:dateCreated |
1997-1-2
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pubmed:abstractText |
Purtilo's syndrome or X-linked lymphoproliferative syndrome (XLP) is a rare genetic disorder affecting boys who have a selective immunodeficit towards Epstein Barr Virus (EBV) and who develop extremely severe forms of EBV infection, of which there are four major types: severe or fatal infectious mononucleosis (60 p. 100), lymphoma (23 p. 100), acquired hypo- or agamaglobulinemia (25 p. 100) and anemia or pancytopenia. We report a case of vasculitis (cutaneous and neurologic) which led to the discovery of a selective immunodeficit towards EBV, similar to Purtilo's syndrome.
|
pubmed:language |
fre
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0151-9638
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
123
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
387-92
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8959062-Adolescent,
pubmed-meshheading:8959062-Herpesviridae Infections,
pubmed-meshheading:8959062-Herpesvirus 4, Human,
pubmed-meshheading:8959062-Humans,
pubmed-meshheading:8959062-Immunologic Deficiency Syndromes,
pubmed-meshheading:8959062-Male,
pubmed-meshheading:8959062-Skin Diseases, Vascular,
pubmed-meshheading:8959062-Syndrome,
pubmed-meshheading:8959062-Treatment Failure,
pubmed-meshheading:8959062-Vasculitis
|
pubmed:year |
1996
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pubmed:articleTitle |
[Cutaneous and neurologic vasculitis disclosing EBV-selective immunodeficiency].
|
pubmed:affiliation |
CHU de Nantes, Hötel-Dieu.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|