Abstract
Although advances in immunosuppressive therapy have allowed prolonged patient survival, immune dysregulation observed in these patients has increased. We report an 11-year-old female heart transplant recipient in whom Glanzmann thrombasthenia was identified as part of a "multiple autoantibody syndrome" manifesting sequentially as autoimmune hemolytic anemia, thrombocytopenia, and neutropenia.
Original language | English (US) |
---|---|
Pages (from-to) | 672-674 |
Number of pages | 3 |
Journal | Journal of Pediatrics |
Volume | 144 |
Issue number | 5 |
DOIs | |
State | Published - May 2004 |
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health