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 | |
| Publication status | Published - Jan 1 2004 |
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All Science Journal Classification (ASJC) codes
- Immunology and Allergy
- Immunology
Cite this
Hyper-IgE syndrome. / Takada, Hidetoshi; Nomura, Akihiko; Hara, Toshiro.
In: Japanese Journal of Clinical Immunology, Vol. 27, No. 6, 01.01.2004, p. 361-366.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Hyper-IgE syndrome
AU - Takada, Hidetoshi
AU - Nomura, Akihiko
AU - Hara, Toshiro
PY - 2004/1/1
Y1 - 2004/1/1
N2 - 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.
AB - 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.
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UR - http://www.scopus.com/inward/citedby.url?scp=17144393289&partnerID=8YFLogxK
U2 - 10.2177/jsci.27.361
DO - 10.2177/jsci.27.361
M3 - Article
C2 - 15678888
AN - SCOPUS:17144393289
VL - 27
SP - 361
EP - 366
JO - Immunological Medicine
JF - Immunological Medicine
SN - 0911-4300
IS - 6
ER -