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

• Autores principales: Payman Sadeghi (Autor), Golnaz Ghazizadeh Esslami (Autor), Hassan Rokni-Zadeh (Autor), Majid Changi-Ashtiani (Autor), Reihaneh Mohsenipour (Autor)
• Formato: Libro
• Publicado: BMC, 2022-11-01T00:00:00Z.
• Materias: article
• Acceso en línea: 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...