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 |
|---|---|
| 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 |
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health