Clinical Manifestations and Pathophysiological Mechanisms of the Wiskott-Aldrich Syndrome


The Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder originally described by Dr. Alfred Wiskott in 1937 and Dr. Robert Aldrich in 1954 as a familial disease characterized by infections, bleeding tendency, and eczema. Today, it is well recognized that the syndrome has a wide clinical spectrum ranging from mild, isolated thrombocytopenia to full… (More)
DOI: 10.1007/s10875-017-0453-z


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