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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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| 出版年: | BMC Med Genet |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6134588/ https://ncbi.nlm.nih.gov/pubmed/30208845 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0673-y |
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