Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/63241
Type: Artigo de periódico
Title: Brazilian report on primary immunodeficiencies in children: 166 cases studied over a follow-up time of 15 years
Author: Grumach, AS
Duarte, AJS
BellinatiPires, R
Pastorino, AC
Jacob, CMA
Diogo, CL
CondinoNeto, A
Kirschfink, M
CarneiroSampaio, MMS
Abstract: One hundred sixty-six cases of primary immunodeficiency diseases (PID) (95 males, 71 females), diagnosed according to WHO criteria, have been registered at the Children's Hospital, University of Sao Paulo, Brazil. The following frequencies were found: predominantly humoral defects, 60.8% (n = 101); T cell defects, 4.9% (n = 8): combined ID, 9.6% (n = 16); phagocyte disorders, 18.7% (n = 31); and complement deficiencies, 6% (it = 10). IgA deficiency was the most frequent disorder (n = 60), followed by transient hypogammaglobulinemia (n = 14), chronic granulomatous disease (ii = 14), and X-linked agammaglobulinemia (n = 9). In comparison to other (national) reports, we observed higher relative frequencies of phagocyte and complement deficiencies. Recurrent infections were the cause of death in 12.7%. Allergic symptoms were observed in 41%, mainly in IEA-deficient, hypogammaglobulinemic. or hyper-IEE patients, and autoimmune disorders in 5%, predominantly in IgA and complement deficiencies. Five patients suffered from BCG dissemination: two of them died. This is the first Brazilian report on PID over an observation time of 15 years.
Subject: primary immunodeficiency
immunologic diseases
children
immunology
Editor: Plenum Publ Corp
Rights: fechado
Identifier DOI: 10.1023/A:1027335000994
Date Issue: 1997
Appears in Collections:Unicamp - Artigos e Outros Documentos

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