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

• Egile Nagusiak: Payman Sadeghi (Egilea), Golnaz Ghazizadeh Esslami (Egilea), Hassan Rokni-Zadeh (Egilea), Majid Changi-Ashtiani (Egilea), Reihaneh Mohsenipour (Egilea)
• Formatua: Liburua
• Argitaratua: BMC, 2022-11-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: 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...