Change in Referral Diagnoses and Diagnostic Delay in Hypogammaglobulinaemic Patients during 28 Years in a Single Referral Centre

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F10%3A%230000485" target="_blank" >RIV/00159816:_____/10:#0000485 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14110/10:00051417
Result on the web
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DOI - Digital Object Identifier
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Result language
angličtina
Original language name
Change in Referral Diagnoses and Diagnostic Delay in Hypogammaglobulinaemic Patients during 28 Years in a Single Referral Centre
Original language description
The classical clinical manifestation of untreated immunoglobulin deficiency comprises predominantly recurrent and complicated respiratory tract infections. Before the 1980s, little was known about the clinical manifestation of immunodeficiency in the general medical population, and also the availability of serum immunoglobulin laboratory determination was not sufficient, leading to a significant diagnostic delay. Our observation documents improved awareness of immunodeficiencies among physicians. It issupposed that earlier diagnosis will prevent complications, improve the quality of life and even survival of hypogammaglobulinaemic patients
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FN - Epidemiology, infection diseases and clinical immunology
OECD FORD branch
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Project
<a href="/en/project/NS10398" target="_blank" >NS10398: Significance of TACI mutations and lymphocyte subpopulations in pathogenesis of selective IgA deficiency</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2010
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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