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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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Detalhes bibliográficos
Main Authors: Yenicesu, İdil, Geneviève, De Saint Basile, Emeksiz, Hamdi Cihan, Dalgıç, Buket
Formato: Artigo
Idioma:Inglês
Publicado em: Galenos Publishing 2012
Assuntos:
Acesso em linha: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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