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Title: Wiscott Aldrich syndrome with oral involvement: a case report. Author: Reddy SS, Binnal A. Journal: J Dent Child (Chic); 2011; 78(1):49-52. PubMed ID: 22041009. Abstract: 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.[Abstract] [Full Text] [Related] [New Search]