Familial Hemophagocytic Lymphohistiocytosis May Present during Adulthood: Clinical and Genetic Features of a Small Series

Familial Hemophagocytic lymphohistiocytosis (FHL) is a rare immune deficiency with defective cytotoxic function. The age at onset is usually young and the natural course is rapidly fatal if untreated. A later onset of the disease has been sporadically reported even in adolescents and adults. We repo...

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Detalles Bibliográficos
Autores principales: Sieni, Elena, Cetica, Valentina, Piccin, Andrea, Gherlinzoni, Filippo, Sasso, Ferdinando Carlo, Rabusin, Marco, Attard, Luciano, Bosi, Alberto, Pende, Daniela, Moretta, Lorenzo, Aricò, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436758/
https://www.ncbi.nlm.nih.gov/pubmed/22970278
http://dx.doi.org/10.1371/journal.pone.0044649

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