Source:http://linkedlifedata.com/resource/pubmed/id/17103011
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2006-11-19
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pubmed:abstractText |
Hyper-IgD and periodic fever syndrome (HIDS) is a hereditary autoinflammatory syndrome, characterized by recurrent inflammatory attacks. Treatment of HIDS is difficult. Recently, the IL-1ra analogue anakinra was reported to be successful in aborting the IgD inflammatory attacks in a vaccination model. We report a clinical case of spectacular reduction of febrile attacks in a severe HIDS patient.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1573-2665
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
763
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pubmed:dateRevised |
2007-3-21
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pubmed:meshHeading |
pubmed-meshheading:17103011-Fever,
pubmed-meshheading:17103011-Humans,
pubmed-meshheading:17103011-Hypergammaglobulinemia,
pubmed-meshheading:17103011-Immunoglobulin D,
pubmed-meshheading:17103011-Inflammation,
pubmed-meshheading:17103011-Interleukin 1 Receptor Antagonist Protein,
pubmed-meshheading:17103011-Syndrome
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pubmed:year |
2006
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pubmed:articleTitle |
Anakinra is safe and effective in controlling hyperimmunoglobulinaemia D syndrome-associated febrile crisis.
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pubmed:affiliation |
AP-HM Timone-Enfants, F-13385, Marseilles Cedex 05, France.
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pubmed:publicationType |
Journal Article,
Case Reports
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