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Prevalence of Primary Immunodeficiency in Korea

Authors
Rhim, Jung WooKim, Kyung HyoKim, Dong SooKim, Bong SeongKim, Jung SooKim, Chang HwiKim, Hwang MinPark, Hee JuPai, Ki SooSon, Byong KwanShin, Kyung SueOh, Moo YoungWoo, Young JongYoo, YoungLee, Kun SooLee, Kyung YilLee, Chong GukLee, Joon SungChung, Eun HeeChoi, Eun HwaHahn, Youn SooPark, Hyun YoungKim, Joong Gon
Issue Date
7월-2012
Publisher
KOREAN ACAD MEDICAL SCIENCES
Keywords
Primary Immunodeficiencies; Registry; Korea
Citation
JOURNAL OF KOREAN MEDICAL SCIENCE, v.27, no.7, pp.788 - 793
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF KOREAN MEDICAL SCIENCE
Volume
27
Number
7
Start Page
788
End Page
793
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/108092
DOI
10.3346/jkms.2012.27.7.788
ISSN
1011-8934
Abstract
This study represents the first epidemiological study based on the national registry of primary immunodeficiencies (PID) in Korea. Patient data were collected from 23 major hospitals. A total of 152 patients with PID (under 19 yr of age), who were observed from 2001 to 2005, have been entered in this registry. The period prevalence of PID in Korea in 2005 is 11.25 per million children. The following frequencies were found: antibody deficiencies, 53.3% (n = 81), phagocytic disorders, 28.9% (n = 44); combined immunodeficiencies, 13.2% (n = 20); and T cell deficiencies, 4.6% (n = 7). Congenital agammaglobulinemia (n = 21) and selective IgA deficiency (n = 21) were the most frequently reported antibody deficiency. Other reported deficiencies were common variable immunodeficiencies (n = 16), X-linked agammaglobulinemia (n = 15), IgG subclass deficiency (n = 4). Phagocytic disorder was mostly chronic granulomatous disease. A small number of patients with Wiskott-Aldrich syndrome, hyper-IgE syndrome, and severe combined immunodeficiency were also registered. Overall, the most common first manifestation was pneumonia. This study provides data that permit a more accurate estimation PID patients in Korea.
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