Abstract
Congenital dyserythropoietic anemia (CDA) is a rare group of inherited bone marrow disorders characterized by anemia with ineffective erythropoiesis. We report 3 siblings from a family known to have CDA type I who presented with persistent pulmonary hypertension of the newborn (PPHN). We suggest that the diagnosis of CDA type I should be considered in any neonate with PPHN and anemia.
Original language | English |
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Pages (from-to) | 553-555 |
Number of pages | 3 |
Journal | Journal of Pediatrics |
Volume | 136 |
Issue number | 4 |
DOIs | |
State | Published - 1 Jan 2000 |
Externally published | Yes |