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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Baishideng Publishing Group Inc
2021
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| Materias: | |
| 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 |