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 › peer-review

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

Access to Document

10.2177/jsci.27.361

Cite this

@article{0d8928e5a7214ea3b391daf74d2573db,

title = "Hyper-IgE syndrome",

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.",

author = "Hidetoshi Takada and Akihiko Nomura and Toshiro Hara",

note = "Funding Information: This work is supported by Grants-in-Aid 19390282 , 20060009 , and 21659253 from the Japanese Ministry of Education, Culture, Sports, Science and Technology , and Research on Intractable Diseases from the Ministry of Health, Labor and Welfare , the Uehara Foundation , Naito Foundation , and the Mother and Child Health Foundation .",

year = "2004",

doi = "10.2177/jsci.27.361",

language = "English",

volume = "27",

pages = "361--366",

journal = "Immunological Medicine",

issn = "0911-4300",

publisher = "Taylor and Francis Ltd.",

number = "6",

}

TY - JOUR

T1 - Hyper-IgE syndrome

AU - Takada, Hidetoshi

AU - Nomura, Akihiko

AU - Hara, Toshiro

N1 - Funding Information: This work is supported by Grants-in-Aid 19390282 , 20060009 , and 21659253 from the Japanese Ministry of Education, Culture, Sports, Science and Technology , and Research on Intractable Diseases from the Ministry of Health, Labor and Welfare , the Uehara Foundation , Naito Foundation , and the Mother and Child Health Foundation .

PY - 2004

Y1 - 2004

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.

UR - http://www.scopus.com/inward/record.url?scp=17144393289&partnerID=8YFLogxK

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 -

Hyper-IgE syndrome

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this