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
โฆ LIBER โฆ
Chronic thrombocytopenia in an immunodeficient patient with hemophilia A
โ Scribed by Hach, Viola ;Bergmann, L. ;Scharrer, I. ;Mitrou, P. ;Mueller-Eckhardt, C.
- Book ID
- 104720650
- Publisher
- Springer-Verlag
- Year
- 1985
- Weight
- 341 KB
- Volume
- 50
- Category
- Article
- ISSN
- 1432-0584
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