Familial hemophagocytic lymphohistiocytosis type 2 in a female Chinese neonate: A case report and review of the literature

BACKGROUND: Familial hemophagocytic lymphohistiocytosis type 2 (FHL2) is a rare genetic disorder presenting with fever, hepatosplenomegaly, and pancytopenia secondary to perforin-1 (PRF1) mutation. FLH2 has been described in Chinese but usually presents after 1 year old. We describe a female Chinese...

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Detalles Bibliográficos
Autores principales: Bi, Shao-Hua, Jiang, Liang-Liang, Dai, Li-Ying, Wang, Li-Li, Liu, Guang-Hui, Teng, Ru-Jeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316947/
https://www.ncbi.nlm.nih.gov/pubmed/34368327
http://dx.doi.org/10.12998/wjcc.v9.i21.6056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316947/
https://www.ncbi.nlm.nih.gov/pubmed/34368327
http://dx.doi.org/10.12998/wjcc.v9.i21.6056

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