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Platelet dysfunction in a patient with the Opitz (BBBG) syndrome.
Authors:R Kapoor  G M Rodgers
Affiliation:Division of Hematology and Oncology, University of Utah School of Medicine, Salt Lake City 84132.
Abstract:
An 11-year-old girl with Opitz (BBBG) syndrome presented with a bleeding disorder. Studies showed an immune-mediated qualitative platelet dysfunction in the absence of thrombocytopenia. This is the first report of hemostatic dysfunction in a patient with the Opitz (BBBG) syndrome. This report considers the possible relationship of the platelet dysfunction to the Opitz (BBBG) syndrome and its treatment.
Keywords:
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