Sustained remission of immune-mediated red cell aplasia in a child after intravenous administration of gamma globulin

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Abstract

A 4-year-old white boy with immune-mediated red cell aplasia and severe anemia was given high intravenous doses of γ-globulin. The therapy was well tolerated and followed by complete resolution of the inhibition of erythropolesis with no recurrence of diseases. Eight months after discontinuation of treatment, the patient has a normal complete blood cell count.

Original languageEnglish
Pages (from-to)403-405
Number of pages3
JournalJournal of Pediatrics
Volume125
Issue number3
DOIs
Publication statusPublished - 1994

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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