Article
Clinical Features and Outcomes of 23 Patients with Wiskott-Aldrich Syndrome: A Single-Center Experience
Turkish journal of haematology : official journal of Turkish Society of Haematology - 19 Nov 2020
Haskoloğlu Şule, Öztürk Ayşenur, Öztürk Gökcan, Kostel Bal Sevgi, İslamoğlu Candan, Baskın Kübra, Ceylaner Serdar, Tufan Satıroğlu Lale, Doğu Figen, İkincioğulları Aydan
Abstract excerpt
Objective: Wiskott-Aldrich syndrome (WAS) is an X-linked primary immune deficiency characterized by microthrombocytopenia, eczema, and recurrent infections. We aimed to evaluate the clinical features and outcomes of a WAS cohort. Materials and Methods: We retrospectively evaluated the clinical courses, immunological features, treatments, and outcomes in a total of 23 WAS patients together with data related to 11...
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