Carregant...
Hemophagocytic lymphohistiocytosis complicated by polyserositis: A case report
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare group of disorders of immune dysregulation characterized by clinical symptoms of severe inflammation. There are basically two types of clinical scenarios: Familial HLH and sporadic HLH. It is thought that the syndrome is implicated in th...
Guardat en:
| Publicat a: | World J Clin Cases |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Baishideng Publishing Group Inc
2019
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6795728/ https://ncbi.nlm.nih.gov/pubmed/31624756 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v7.i19.3069 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|