First Report of the Hyper-IgM Syndrome Registry of the Latin American Society for Immunodeficiencies: Novel Mutations, Unique Infections, and Outcomes

Author:

Cabral-Marques Otavio,Klaver Stefanie,Schimke Lena F,Ascendino Évelyn H,Khan Taj Ali,Pereira Paulo Vítor Soeiro,Falcai Angela,Vargas-Hernández Alexander,Santos-Argumedo Leopoldo,Bezrodnik Liliana,Moreira Ileana,Seminario Gisela,Di Giovanni Daniela,Raccio Andrea Gómez,Porras Oscar,Weber Cristina Worm,Ferreira Janaíra Fernandes,Tavares Fabiola Scancetti,de Carvalho Elisa,Valente Claudia França Cavalcante,Kuntze Gisele,Galicchio Miguel,King Alejandra,Rosário-Filho Nelson Augusto,Grota Milena Baptistella,dos Santos Vilela Maria Marluce,Di Gesu Regina Sumiko Watanabe,Lima Simone,de Souza Moura Leiva,Talesnik Eduardo,Mansour Eli,Roxo-Junior Pérsio,Aldave Juan Carlos,Goudouris Ekaterine,Pinto-Mariz Fernanda,Berrón-Ruiz Laura,Staines-Boone Tamara,Calderón Wilmer O. Córdova,del Carmen Zarate-Hernández María,Grumach Anete S.,Sorensen Ricardo,Durandy Anne,Torgerson Troy R.,Carvalho Beatriz Tavares Costa,Espinosa-Rosales Francisco,Ochs Hans D.,Condino-Neto Antonio

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Reference51 articles.

1. Notarangelo LD, Duse M, Ugazio AG. Immunodeficiency with hyper-IgM (HIM). Immunodefic Rev. 1992;3(2):101–21.

2. Burtin P. An example of atypical agammaglobulinemia (a case of severe hypogammaglobulinemia with increase of the beta-2 macroglobulin. Rev Fr Etud Clin Biol. 1961;6:286–9.

3. Israel-Asselain R, Burtin P, Chebat J. A new biological disorder: agammaglobulinemia with beta2-macroglobulinemia (a case). Bull Mem Soc Med Hop Paris. 1960;76:519–23.

4. Rosen FS, Kevy SV, Merler E, Janeway CA, Gitlin D. Dysgammaglobulinaemia and recurrent bacterial infection. Lancet. 1961;1(7179):700.

5. Allen RC, Armitage RJ, Conley ME, Rosenblatt H, Jenkins NA, Copeland NG, et al. CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome. Science. 1993;259(5097):990–3.

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