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

Mutations in the genes coding for cytokines, receptors, second messengers, and transcription factors of interferon gamma (IFN-γ) immunity cause Mendelian susceptibility to mycobacterial disease (MSMD). We report the case of a 7-year-old male patient with partial dominant (PD) IFN-γ receptor 1 defici...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413492/
https://www.ncbi.nlm.nih.gov/pubmed/28516082
http://dx.doi.org/10.3389/fped.2017.00075

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