RARE PRIMARY IMMUNODEFICIENCY – HYPER-IgE-SYNDROME: CASE REPORT AND LITERATURE REVIEW

RARE PRIMARY IMMUNODEFICIENCY – HYPER-IgE-SYNDROME: CASE REPORT AND LITERATURE REVIEW

The article is dedicated to one of the rare primary immunodeficiency pathologies – hyper-IgE-syndrome. The authors present a clinical case from their own practice and a literature review on this disease. Inheritance, pathogenesis, clinical manifestations and hyper-IgE-syndrome diagnostics issues are...

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Bibliographic Details
Main Authors: Nikolai Vasil'evich Sobotyuk, E. A. Potrokhova, S. A. Golochalova, S. V. Bochantsev, T. N. Kharlamova, Y. A. Stroylova
Format: Article
Language:Russian
Published: Union of pediatricians of Russia 2013-01-01
Series:Педиатрическая фармакология
Subjects:
primary immunodeficiency
yper-ige-syndrome
inheritance
etiology
pathogenesis
clinical course
diagnostics
treatment
children
Online Access:https://www.pedpharma.ru/jour/article/view/253
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Summary:The article is dedicated to one of the rare primary immunodeficiency pathologies – hyper-IgE-syndrome. The authors present a clinical case from their own practice and a literature review on this disease. Inheritance, pathogenesis, clinical manifestations and hyper-IgE-syndrome diagnostics issues are also examined in the article. The article shows differences of disease course at different inheritance types – autosomal-dominant and autosomal-recessive.
ISSN:1727-5776
2500-3089

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