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Title: Current and emerging treatment options for Wiskott-Aldrich syndrome. Author: Worth AJ, Thrasher AJ. Journal: Expert Rev Clin Immunol; 2015; 11(9):1015-32. PubMed ID: 26159751. Abstract: Wiskott-Aldrich syndrome is a life-threatening primary immunodeficiency associated with a bleeding tendency, eczema and a high incidence of autoimmunity and malignancy. Stem cell transplantation offers the opportunity of cure for all these complications, and over the past 35 years there has been a remarkable improvement in survival following this treatment. Here, we review advances in management of clinical complications pre- and post-transplant, as well as discuss the morbidity Wiskott-Aldrich syndrome patients experience following treatment. For patients with a poorly matched stem cell donor, recent gene therapy trials demonstrate encouraging results and the potential of low-toxicity therapy for all patients.[Abstract] [Full Text] [Related] [New Search]