| Literature DB >> 17103011 |
M Cailliez1, F Garaix, C Rousset-Rouvière, D Bruno, I Kone-Paut, J Sarles, B Chabrol, M Tsimaratos.
Abstract
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.Entities:
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Year: 2006 PMID： 17103011 DOI： 10.1007/s10545-006-0408-7
Source DB: PubMed Journal: J Inherit Metab Dis ISSN： 0141-8955 Impact factor: 4.982