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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...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Galenos Publishing
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3986752/ https://ncbi.nlm.nih.gov/pubmed/24744671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5505/tjh.2012.62134 |
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