Définition:
A rare, X-linked immunodeficiency syndrome characterized by eczema, thrombocytopenic purpura, and recurrent pyogenic infection. It is seen exclusively in young boys. Typically, levels are low and and levels are elevated. Lymphoreticular malignancies are common.
Synonyme(s):
Maladie de Wiskott-Aldrich /
Syndrome Aldrich /