Hyper-Immunoglobulin A in the Hyperimmunoglobulinemia D Syndrome

The hyperimmunoglobulinemia D syndrome (HIDS) is an autosomal recessive disorder characterized by recurrent febrile attacks with abdominal, articular, and skin manifestations. Apart from elevated immunoglobulin D (IgD) levels (>100 IU/ml), there are high IgA levels in the majority of cases. Mutation...

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Dades bibliogràfiques
Publicat a:	Clin Diagn Lab Immunol
Autors principals:	Klasen, Ina S., Göertz, Joop H. C., van de Wiel, Gertrude A. S., Weemaes, Corry M. R., van der Meer, Jos W. M., Drenth, Joost P. H.
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Microbiology (ASM) 2001
Matèries:	Immune-Mediated Responses and Disorders
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC96011/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11139196/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/CDLI.8.1.58-61.2001
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Hyper-Immunoglobulin A in the Hyperimmunoglobulinemia D Syndrome

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