Familial Hemophagocytic Lymphohistiocytosis Secondary to PRF1 Mutation

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome that causes systemic inflammation which can progress to multiorgan failure and death. Symptoms and signs commonly seen in HLH include high fever, hepatosplenomegaly, pancytopenia, and hypertriglyceridemia. This...

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Detalles Bibliográficos
Autores principales: Alfaraidi, Albaraa T., Alqarni, Abdulaziz A., Aqeel, Mohammed T., Albalawi, Turki A., Hejazi, Ahmed S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8731261/
https://www.ncbi.nlm.nih.gov/pubmed/35003815
http://dx.doi.org/10.1155/2021/7213939

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8731261/
https://www.ncbi.nlm.nih.gov/pubmed/35003815
http://dx.doi.org/10.1155/2021/7213939

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