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Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease characterized by some clinical signs (e.g., non-remitting fever, hepatosplenomegaly) and laboratory findings (e.g., cytopenia, increased ferritin level, hypofibrinogenemia, lipid disorders, coagulopathy, and multiple...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675162/ https://www.ncbi.nlm.nih.gov/pubmed/36401200 http://dx.doi.org/10.1186/s12887-022-03746-9 |