Primary immunodeficiency diseases in Latin America: the second report of the LAGID registry

Primary immunodeficiency diseases in Latin America: the second report of the LAGID registry

Author Leiva, Lily E. Google Scholar
Zelazco, Marta Google Scholar
Oleastro, Matias Google Scholar
Carneiro-Sampaio, Magda Google Scholar
Condino-Neto, Antonio Google Scholar
Costa-Carvalho, Beatriz Tavares Google Scholar
Grumach, Anete Sevciovic Google Scholar
Quezada, Arnoldo Google Scholar
Patino, Pablo Google Scholar
Franco, Jose Luis Google Scholar
Porras, Oscar Google Scholar
Rodriguez, Francisco Javier Google Scholar
Espinosa-Rosales, Francisco Javier Google Scholar
Espinosa-Padilla, Sara Elva Google Scholar
Almillategui, Diva Google Scholar
Martinez, Celia Google Scholar
Tafur, Juan Rodriguez Google Scholar
Valentin, Marilyn Google Scholar
Benarroch, Lorena Google Scholar
Barroso, Rosy Google Scholar
Sorensen, Ricardo U. Google Scholar
Institution Louisiana State Univ
Hosp Nacl Ped Juan P Garrahan
Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Univ Chile
Univ Antioquia
Hosp Nacl Ninos Dr Carlos Saenz Herrera
Inst Nacl Seguridad Social
Inst Nacl Pediat
Hosp Ninos Panama
Inst Invest Ciencias Salud
Univ Nacl Mayor San Marcos
Hosp Pediatr Pereira Rossell
Hosp Clin
Clin Leopoldo Aguerrevere
Abstract This is the second report on the continuing efforts of LAGID to increase the recognition and registration of patients with primary immunodeficiency diseases in 12 Latin American countries: Argentina, Brazil, Chile, Colombia, Costa Rica, Honduras, Mexico, Panama, Paraguay, Peru, Uruguay, and Venezuela. This report reveals that from a total of 3321 patients registered, the most common form of primary immunodeficiency disease was predominantly antibody deficiency (53.2%) with IgA deficiency reported as the most frequent phenotype. This category was followed by 22.6% other well-defined ID syndromes, 9.5% combined T- and B-cell inmunodeficiency, 8.6% phagocytic disorders, 3.3% diseases of immune dysregulation, and 2.8% complement deficiencies. All countries that participated in the first publication in 1998 reported an increase in registered primary immunodeficiency cases, ranging between 10 and 80%. A comparison of the estimated minimal incidence of X-linked agammaglobulinemia, chronic granulomatous disease, and severe combined immunodeficiency between the first report and the present one shows an increase in the reporting of these diseases in all countries. in this report, the estimated minimal incidence of chronic granulomatous disease was between 0.72 and 1.26 cases per 100,000 births in Argentina, Chile, Costa Rica, and Uruguay and the incidence of severe combined immunodeficiency was 1.28 and 3.79 per 100,000 births in Chile and Costa Rica, respectively. However, these diseases are underreported in other participating countries. in addition to a better diagnosis of primary immunodeficiency diseases, more work on improving the registration of patients by each participating country and by countries that have not yet joined LAGID is still needed.
Keywords primary immunodeficiency
Latin America
LAGID
immunodeficiency epidemiology
Language English
Date 2007-01-01
Published in Journal of Clinical Immunology. New York: Springer/plenum Publishers, v. 27, n. 1, p. 101-108, 2007.
ISSN 0271-9142 (Sherpa/Romeo, impact factor)
Publisher Springer
Extent 101-108
Origin http://dx.doi.org/10.1007/s10875-006-9052-0
Access rights Closed access
Type Article
Web of Science ID WOS:000244093500009
URI http://repositorio.unifesp.br/handle/11600/29368

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