Tumour necrosis factor receptor-associated periodic syndrome caused by a rare mutation in the TNFRSF1A gene, and with excellent response to etanercept treatment

Tumour necrosis factor receptor-associated periodic syndrome caused by a rare mutation in the TNFRSF1A gene, and with excellent response to etanercept treatment

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Veröffentlicht in:Clinical and experimental rheumatology 2009-09, Vol.27 (5), p.890
Hauptverfasser: Cantarini, L, Lucherini, O M, Galeazzi, M, Fanti, F, Simonini, G, Baldari, C T, Laghi Pasini, F, De Martino, M, Cimaz, R
Format: Artikel
Sprache:eng
Schlagworte:
Child
Etanercept
Female
Hereditary Autoinflammatory Diseases - diagnosis
Hereditary Autoinflammatory Diseases - drug therapy
Hereditary Autoinflammatory Diseases - genetics
Humans
Immunoglobulin G - therapeutic use
Immunologic Factors - therapeutic use
Mutation
Receptors, Tumor Necrosis Factor - therapeutic use
Receptors, Tumor Necrosis Factor, Type I - genetics
Syndrome
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ISSN:0392-856X