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Hindi Case Report, J Immunodefic Disor Vol: 1 Issue: 4
Recurrent Salmonellosis in a Child with Complete IL-12Rβ1 Deficiency
| Mohammad Faizan Zahid1, Syed Asad Ali2, Fyezah Jehan2, Abdul Gaffar Billo2, Jean-Laurent Casanova3,4,5, Jacinta Bustamante4,5,6, Stephanie Boisson-Dupuis3,4,5 and Fatima Mir2* | |
| 1Medical College, Aga Khan University, Karachi 74800, Pakistan | |
| 2Department of Pediatrics and Child Health, Aga Khan University, Karachi 74800, Pakistan | |
| 3St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, New York, 10065, USA | |
| 4Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U980, Necker Enfants Malades Hospital, Paris, 75015, France, EU | |
| 5University Paris Descartes, Imagine Institute, Paris, 75015, France, EU | |
| 6Center for the Study of Primary Immunodeficiencies, Assistance Publique–Hôpitaux de Paris, Necker Enfants Malades Hospital, Paris, 75015, France, EU | |
| Corresponding author : Fatima Mir Department of Pediatrics and Child Health, Aga Khan University, Stadium Road, PO Box 3500, Karachi 74800, Pakistan Tel: 9221-4864955; Fax: 9221-493-4294 E-mail: fatima.mir@aku.edu |
|
| Received: March 24, 2014 Accepted: May 28, 2014 Published: June 04, 2014 | |
| Citation: Zahid MF, Ali SA, Jehan F, Billoo AG, Casanova JL, et al., (2014) Recurrent Salmonellosis in a Child with Complete IL-12Rß1 Deficiency. J Immunodefic Disor 3:1.doi:10.4172/2324-853X.1000109 |
Abstract
Recurrent Salmonellosis in a Child with Complete IL-12Rβ1 Deficiency
A 3 year old boy presented with fever, abdominal pain and cervical lymphadenopathy. He had previously been treated empirically with anti-tuberculous therapy twice, at age 9 months and 27 months, for peripheral lymphadenopathy. An older sibling died of suspected tuberculous meningitis.