Wiscott Aldrich syndrome with oral involvement: a case report.

Wiskott Aldrich syndrome is an X-linked recessive disorder characterized by thrombocytopenia with microplatelets, eczema, recurrent infections, and predisposition to autoimmune disease and malignancy. It is a rare syndrome, and the incidence rate is approximately 4 in every 1 million live male births with no clear ethnic or racial predilection. The purpose of this paper was to report a case of Wiskott Aldrich syndrome with oral involvement demonstrated by 2 male siblings.