Hemophagocytic lymphohistiocytosis and congenital factor VII deficiency: a case report

BACKGROUND: Hemophagocytic lymfohistiocytosis (HLH) is a rare, life-threatening hyperinflammation, characterized by immune system over-activation resulting in hemophagocytosis. HLH could appear as a primary disease caused by mutations of immune-regulatory genes, or develop as a result of viral or ba...

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Detalles Bibliográficos
Autores principales: Wang, Xiong, Tang, Ning, Chang, Wei, Lu, Yanjun, Li, Dengju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134588/
https://www.ncbi.nlm.nih.gov/pubmed/30208845
http://dx.doi.org/10.1186/s12881-018-0673-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134588/
https://www.ncbi.nlm.nih.gov/pubmed/30208845
http://dx.doi.org/10.1186/s12881-018-0673-y

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