Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn

J Pediatr. 2000 Apr;136(4):553-5. doi: 10.1016/s0022-3476(00)90025-8.

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.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Anemia, Dyserythropoietic, Congenital / diagnosis*
  • Anemia, Dyserythropoietic, Congenital / genetics
  • Arabs
  • Consanguinity
  • Diagnosis, Differential
  • Female
  • Humans
  • Infant, Newborn
  • Israel
  • Male
  • Pedigree
  • Persistent Fetal Circulation Syndrome / diagnosis*
  • Persistent Fetal Circulation Syndrome / genetics