Hemophilia and thrombocytopenia in a patient with impaired cellular immunity. A case report
ITP in hemophiliacs may produce severe bleeding complications. We here report on an eight-year-old boy suffering from severe hemophilia A, who developed ITP and an acquired impaired immune function similar to AIDS. Steroid therapy reverted the thrombocyte count to normal, however it had to be discon...
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Veröffentlicht in: | Blut 1984-06, Vol.48 (6), p.393-395 |
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Sprache: | eng |
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