A Case of Hyperimmunoglobulinemia D Syndrome Successfully Treated with Canakinumab

Hyperimmunoglobulinemia D syndrome is a rare autosomal recessive autoinflammatory disorder caused by mutations in the mevalonate kinase gene (MVK). In a proportion of patients, however, no MVK mutations are detected. Although various standard anti-inflammatory drugs have been tried, until now there...

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Detalles Bibliográficos
Autores principales: Tsitsami, Elena, Papadopoulou, Charis, Speletas, Matthaios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652103/
https://www.ncbi.nlm.nih.gov/pubmed/23691418
http://dx.doi.org/10.1155/2013/795027

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652103/
https://www.ncbi.nlm.nih.gov/pubmed/23691418
http://dx.doi.org/10.1155/2013/795027

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