Multifocal Recurrent Osteomyelitis and Hemophagocytic Lymphohistiocytosis in a Boy with Partial Dominant IFN-γR1 Deficiency: Case Report and Review of the Literature-Reference-Cited by-同舟云学术

Multifocal Recurrent Osteomyelitis and Hemophagocytic Lymphohistiocytosis in a Boy with Partial Dominant IFN-γR1 Deficiency: Case Report and Review of the Literature

Published:2017-05-03 Issue: Volume:5 Page:
ISSN:2296-2360
Container-title:Frontiers in Pediatrics
language:
Short-container-title:Front. Pediatr.

Author:

Staines-Boone Aidé Tamara,Deswarte Caroline,Venegas Montoya Edna,Sánchez-Sánchez Luz María,García Campos Jorge Alberto,Muñiz-Ronquillo Teodoro,Bustamante Jacinta,Espinosa-Rosales Francisco J.,Lugo Reyes Saul Oswaldo

Publisher

Frontiers Media SA

Subject

Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Clinical features of dominant and recessive interferon gamma receptor 1 deficiencies;Dorman;Lancet,2004

2. Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-gamma immunity;Bustamante;Semin Immunol,2014

3. Inherited and acquired immunodeficiencies underlying tuberculosis in childhood;Boisson-Dupuis;Immunol Rev,2015

4. Hemophagocytic lymphohistiocytosis in children: pathogenesis and treatment;Ishii;Front Pediatr,2016

5. HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis;Henter;Pediatr Blood Cancer,2007

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