Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases

• Autori principali: Payman Sadeghi (Autore), Golnaz Ghazizadeh Esslami (Autore), Hassan Rokni-Zadeh (Autore), Majid Changi-Ashtiani (Autore), Reihaneh Mohsenipour (Autore)
• Natura: Libro
• Pubblicazione: BMC, 2022-11-01T00:00:00Z.
• Soggetti: article
• Accesso online: Connect to this object online.

Abstract Background Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease characterized by some clinical signs (e.g., non-remitting fever, hepatosplenomegaly) and laboratory findings (e.g., cytopenia, increased ferritin level, hypofibrinogenemia, lipid disorders, coagulopathy, and m...