[The Spanish Registry of Primary Immunodeficiencies (REDIP)]

التفاصيل البيبلوغرافية
العنوان: [The Spanish Registry of Primary Immunodeficiencies (REDIP)]
المؤلفون: J, Milá Llambí, A, Etxagibel Galdos, N, Matamoros Florí
المصدر: Allergologia et immunopathologia. 29(3)
سنة النشر: 2001
مصطلحات موضوعية: Common Variable Immunodeficiency, Phagocytosis, Agammaglobulinemia, Spain, Immunologic Deficiency Syndromes, Humans, Immunoglobulins, Intravenous, Severe Combined Immunodeficiency, Complement System Proteins, Registries, Granulomatous Disease, Chronic
الوصف: Two thousand and fifty cases (n = 2050) of primary immunodeficiencies (PID) were registered up to February 2001. The Spanish Register for Primary Immunodeficiencies (REDIP) began in 1993. PID nomenclature and diagnostic criteria were made according to the report of the World Health Organization Scientific Group (1999). The most frequent disorders were IgA deficiency (797 registers) and common variable immunodeficiency (CVI) (389), followed by severe combined immunodeficiency and predominantly T cell defects (268), complement deficiencies (207 registers), X-linked agammaglobulinemia (87), IgG subclass deficiency (71), chronic granulomatous disease (64). Gammaglobulin replacement was the therapy in 638 patients (76%) belonging to antibody deficient group. 61 bone marrow transplants were done, 46 severe combined immunodeficiencies, 6 phagocytic disorders and 1 unclassified. Important differences in the number of cases submitted from different country areas were found.
تدمد: 0301-0546
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::24d37e4c2d0b19e1139bf28f8cabd5e1
https://pubmed.ncbi.nlm.nih.gov/11434886
رقم الانضمام: edsair.pmid..........24d37e4c2d0b19e1139bf28f8cabd5e1
قاعدة البيانات: OpenAIRE