Epstein–Barr virus-related hemophagocytic lymphohistiocytosis complicated with coronary artery dilation and acute renal injury in a boy with a novel X-linked inhibitor of apoptosis protein (XIAP) variant: a case report

BACKGROUND: X-linked lymphoproliferative disease (XLP) is a rare inherited X-linked primary immunodeficiency diseases (PID). One such disease, X-linked inhibitor of apoptosis protein (XIAP) deficiency, is characterized by Epstein–Barr virus-related hemophagocytic lymphohistiocytosis (EBV-HLH). Howev...

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Detalles Bibliográficos
Autores principales: Chen, Ru-Yue, Li, Xiao-Zhong, Lin, Qiang, Zhu, Yun, Shen, Yun-Yan, Xu, Qin-Ying, Zhu, Xue-Ming, Bai, Zhen-Jiang, Li, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531141/
https://www.ncbi.nlm.nih.gov/pubmed/33008347
http://dx.doi.org/10.1186/s12887-020-02359-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531141/
https://www.ncbi.nlm.nih.gov/pubmed/33008347
http://dx.doi.org/10.1186/s12887-020-02359-4

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