Systemic aspergillosis in a patient with interferon gamma receptor 1 deficiency; a case report

BACKGROUND: Interferon-gamma receptor deficiency is a heterogeneous spectrum of disease which involves mutations in IFNGR1, IFNGR2 genes, and the downstream signaling proteins such as STAT1. These mutations are associated with immunodeficiency 27 A and 27B, making the patient prone to mycobacterial...

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Detalles Bibliográficos
Autores principales: Esmaeilzadeh, Hossein, Chavoshzadeh, Zahra, Nabavizadeh, Seyed Hesamedin, Alyasin, Soheila, Amanati, Ali, Askarisarvestani, Aida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240762/
https://www.ncbi.nlm.nih.gov/pubmed/37277724
http://dx.doi.org/10.1186/s12887-023-04093-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240762/
https://www.ncbi.nlm.nih.gov/pubmed/37277724
http://dx.doi.org/10.1186/s12887-023-04093-z

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