The Wiskott-Aldrich syndrome: studies of lymphocytes, granulocytes, and platelets
HD Ochs(University of Washington), S. J. Slichter(University of Washington), Lee A. Harker(University of Washington), Wieland E. von Behrens(Bloodworks Northwest), Robert A. Clark(Bloodworks Northwest), RalphJ. Wedgwood(Bloodworks Northwest)
Cited by 327
Abstract
until 6 yr of age.When 6 mo old, the patient developed petechiae, episodes of epistaxis, and a low platelet count was noted (5000-5O OOO/i l).Immune-mediated thrombocytopenia was considered, and he was treated intermittently with steroids without improvement.Following splenectomy at age 5, his bleeding tendency disappeared, although his platelet counts were still low, ranging between
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