Introduction Wiskott-Aldrich Syndrome (WAS) is a rare X-linked primary immunodeficiency characterized by a classic triad of microthrombocytopenia, eczema, and recurrent infections, with a heightened risk of autoimmunity and malignancy (1). This rare X-linked primary immunodeficiency occurs in approximately 1 to 4 per 1,000,000 live male births (2).
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