Primary Immunodeficiency Diseases in Latin America: Epidemiology and Perspectives

نویسندگان

  • Paolo Ruggero Errante
  • Antonio Condino-Neto
چکیده

Primary immunodeficiencies (PID) are genetic disorders of immunity whose incidence varies from 1:250 to 1:1,000,000 depending of disease and study population. Because of incomplete records of immunodeficiency in the world, is estimated that the prevalence of 1:5,000 to 1:100,000 (Geha et al., 2007; Boyle & Buckley, 2007; Notarangelo,et al., 2010). Thus, the PID is a important group to public health as other genetic diseases that rely government support in a neonatal screening program such phenylketonuria (PKU) with incidence of 1/15.000 (de Carvalho et al., 2007) and congenital hypothyroidism, with incidence of 1/4.000 (American Academy of Pediatrics, 1993; Olivieri, 2009). The PID are classified in defective immune deficiency prevalent in predominantly antibody; combined immunodeficiencies, cellular immunodeficiencies, phagocyte defects, immune deficiencies associated with lymphoproliferative diseases, and deficiencies of complement system or secondary immunodeficiencies associated with other diseases. This classification is updated periodically by the International Union of Immunological Societies (IUIS), associated with the World Health Organization (WHO) (Geha et al., 2007; Notarangelo,et al., 2010).

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تاریخ انتشار 2012