Table 1
Required criteria 
    Chronic nonmalignant lymphadenopathy and/or splenomegaly 
    Increased peripheral CD3+TCRαβ+CD4CD8 (DNT) cells 
    Lymphocyte apoptosis defect 
Supporting criteria 
    Family history of ALPS 
    Characteristic histopathology 
    Autoimmune manifestations 
Required criteria 
    Chronic nonmalignant lymphadenopathy and/or splenomegaly 
    Increased peripheral CD3+TCRαβ+CD4CD8 (DNT) cells 
    Lymphocyte apoptosis defect 
Supporting criteria 
    Family history of ALPS 
    Characteristic histopathology 
    Autoimmune manifestations 

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