Abstract
A 4-year-old white boy with immune-mediated red cell aplasia and severe anemia was given high intravenous doses of gamma-globulin. The therapy was well tolerated and followed by complete resolution of the inhibition of erythropoiesis with no recurrence of disease. Eight months after discontinuation of treatment, the patient has a normal complete blood cell count.
Lingua originale | Inglese |
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pagine (da-a) | 403-405 |
Numero di pagine | 3 |
Rivista | THE JOURNAL OF PEDIATRICS |
Volume | 125 |
Numero di pubblicazione | 3 |
DOI | |
Stato di pubblicazione | Pubblicato - 1994 |
All Science Journal Classification (ASJC) codes
- Pediatria, Perinatologia e Salute del Bambino
Keywords
- Pure / pathology
- Red-Cell Aplasia