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Common variable immunodeficiency: epidemiology, pathogenesis, clinical manifestations, diagnosis, classification, and management
Yazdani, R; Habibi, S; Sharifi, L; Azizi, G; Abolhassani, H; Olbrich, P; Aghamohammadi, Asghar.
Affiliation
  • Yazdani, R; Tehran University of Medical Science. Children's Medical Center. Pediatrics Center of Excellence. Research Center for Immunodeficiencies. Tehran. Iran
  • Habibi, S; Tehran University of Medical Science. Children's Medical Center. Pediatrics Center of Excellence. Research Center for Immunodeficiencies. Tehran. Iran
  • Sharifi, L; Tehran University of Medical Sciences. Uro-Oncology Research Center. Tehran. Iran
  • Azizi, G; Alborz University of Medical Sciences. Non-Communicable Diseases Research Center. Karaj. Iran
  • Abolhassani, H; Iran University of Medical Science. Research Center for Primary Immunodeficiencies. Tehran. Iran
  • Olbrich, P; Hospital Virgen del Rocío. Sección de Infectología e Inmunopatología. Unidad de Pediatría. Seville. Spain
  • Aghamohammadi, Asghar; Tehran University of Medical Science. Children's Medical Center. Pediatrics Center of Excellence. Research Center for Immunodeficiencies. Tehran. Iran
J. investig. allergol. clin. immunol ; 30(1): 14-34, 2020. tab, graf
Article in English | IBECS | ID: ibc-194103
Responsible library: ES1.1
Localization: BNCS
ABSTRACT
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by hypogammaglobulinemia and increased susceptibility to recurrent bacterial infections. It is the most frequent symptomatic antibody deficiency, with a wide variety of infectious and noninfectious complications. Numerous studies have demonstrated that immunological and genetic defects are involved in the pathogenesis of CVID. However, in most cases, the genetic background of the disease remains unidentified. This review aims to discuss various aspects of CVID, including epidemiology, pathogenesis, symptoms, diagnosis, classification, and management
RESUMEN
La inmunodeficiencia variable común (CVID) es un trastorno heterogéneo caracterizado por una hipogammaglobulinemia y por una mayor susceptibilidad a infecciones bacterianas recurrentes. Se trata de la inmunodeficiencia humoral sintomática más frecuente y cursa con una extensa variedad de complicaciones infecciosas y no infecciosas. En la patogenia de la CVID están involucrados diferentes defectos inmunológicos y genéticos. Sin embargo, en la mayoría de los casos, el fondo genético de la enfermedad permanece sin identificar. Esta revisión tiene como objetivo discutir diferentes aspectos de la CVID, incluyendo epidemiología, patogenia, síntomas, diagnóstico, clasificaciones y tratamiento de la enfermedad
Subject(s)

Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Immunoglobulins, Intravenous / Common Variable Immunodeficiency Limits: Animals / Humans Language: English Journal: J. investig. allergol. clin. immunol Year: 2020 Document type: Article Institution/Affiliation country: Alborz University of Medical Sciences/Iran / Hospital Virgen del Rocío/Spain / Iran University of Medical Science/Iran / Tehran University of Medical Science/Iran / Tehran University of Medical Sciences/Iran

Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Immunoglobulins, Intravenous / Common Variable Immunodeficiency Limits: Animals / Humans Language: English Journal: J. investig. allergol. clin. immunol Year: 2020 Document type: Article Institution/Affiliation country: Alborz University of Medical Sciences/Iran / Hospital Virgen del Rocío/Spain / Iran University of Medical Science/Iran / Tehran University of Medical Science/Iran / Tehran University of Medical Sciences/Iran
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