Hyper-IgE syndrome

Hidetoshi Takada; Akihiko Nomura; Toshiro Hara

doi:10.2177/jsci.27.361

Hyper-IgE syndrome

Hidetoshi Takada, Akihiko Nomura, Toshiro Hara

Faculty of Medical Sciences

Research output: Contribution to journal › Article

2 Citations (Scopus)

Abstract

Hyperimmunoglobulin-E syndrome is one of the primary immunodeficiency with the manifestations of recurrent infections especially with Staphylococcus aureus, characteristic facies, hyperextensibility of joints, multiple bone fractures, scoliosis, and delayed shedding of the primary teeth. It is a multisystem disease of autosomal dominant inheritance. Recently, a new type of hyper-IgE syndrome with autosomal recessive inheritance was identified. Although Th1/Th2 imbalance has been suspected to be a cause of this diesease, it is not clarified yet.

Original language	English
Pages (from-to)	361-366
Number of pages	6
Journal	Japanese Journal of Clinical Immunology
Volume	27
Issue number	6
DOIs	https://doi.org/10.2177/jsci.27.361
Publication status	Published - 2004

All Science Journal Classification (ASJC) codes

Immunology and Allergy
Immunology

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Takada, H., Nomura, A., & Hara, T. (2004). Hyper-IgE syndrome. Japanese Journal of Clinical Immunology, 27(6), 361-366. https://doi.org/10.2177/jsci.27.361

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