X-linked Agammaglobulinemia in Community-acquired Pneumonia Cases Revealed by Immunoglobulin Level Screening at Hospital Admission
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F13%3A10209702" target="_blank" >RIV/00216208:11110/13:10209702 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14740/13:00072825 RIV/00216208:11130/13:10209702 RIV/00064211:_____/13:#0000247
Result on the web
<a href="http://dx.doi.org/10.1055/s-0033-1354415" target="_blank" >http://dx.doi.org/10.1055/s-0033-1354415</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1055/s-0033-1354415" target="_blank" >10.1055/s-0033-1354415</a>
Alternative languages
Result language
angličtina
Original language name
X-linked Agammaglobulinemia in Community-acquired Pneumonia Cases Revealed by Immunoglobulin Level Screening at Hospital Admission
Original language description
In children with primary immunodeficiencies, the onset of symptoms precedes the diagnosis and the initiation of appropriate treatment by months or years. This delay in diagnosis is due to the fact that while these disorders are rare, some of the infections seen in immunodeficient patients are common. Defective antibody production represents the largest group among these disorders, with otitis, sinusitis and pneumonia as the most frequent initial manifestation. We performed a prospective study of humoralimmunity in children hospitalized due to community-acquired pneumonia in tertiary care hospital. Out of 254 patients (131 boys, 123 girls, median age 4.5 years) recruited over 3 years, we found 2 boys (age 11 and 21 months) lacking serum immunoglobulinsand circulating B cells. Subsequent genetic analysis confirmed diagnosis of X-linked agammaglobulinemia. Despite their immunodeficiency, the pneumonia was uncomplicated in both patients and did not call for immunological evaluation. Howe
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FG - Paediatrics
OECD FORD branch
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Result continuities
Project
<a href="/en/project/EE2.3.20.0045" target="_blank" >EE2.3.20.0045: Support of Professional Growth and International Integration of Research Teams in the Filed of Molecular Medicine</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Klinische Padiatrie
ISSN
0300-8630
e-ISSN
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Volume of the periodical
225
Issue of the periodical within the volume
6
Country of publishing house
DE - GERMANY
Number of pages
4
Pages from-to
339-342
UT code for WoS article
000327015800010
EID of the result in the Scopus database
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