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Familial Hemophagocytic Lymphohistiocytosis with A665G Perforin Gene Mutation: A Case Report
Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous disease. Presentation of the disease such as primarily fever, hepatosplenomegaly, and cytopenia, which are the results of functional degradation in cytotoxic T-lymphocytes and natural killer cells, activation of macroph...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Galenos Publishing
2012
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986752/ https://www.ncbi.nlm.nih.gov/pubmed/24744671 http://dx.doi.org/10.5505/tjh.2012.62134 |