Anemia in the Neonate: The Differential Diagnosis and Treatment

Pediatr Ann. 2015 Jul;44(7):e159-63. doi: 10.3928/00904481-20150710-08.

Abstract

Anemia is a common problem in the neonatal period. Presenting symptoms may suggest numerous possible diagnoses ranging from anemia seen as a normal part of development to anemia due to critical pathology. An illustrative case is presented to highlight the appropriate evaluation of the neonate with significant anemia. Several important features of the evaluation of neonatal anemia are highlighted. The constellation of signs and symptoms that occur in conjunction with the anemia are critical for the evaluation. The evaluation should be performed in a step-wise process that starts by eliminating common causes of anemia. Manual review of the peripheral blood smear with a hematologist can be helpful.

Publication types

  • Case Reports

MeSH terms

  • Anemia, Hemolytic, Congenital Nonspherocytic / diagnosis*
  • Anemia, Hemolytic, Congenital Nonspherocytic / genetics
  • Anemia, Hemolytic, Congenital Nonspherocytic / therapy
  • Anemia, Neonatal / diagnosis*
  • Anemia, Neonatal / genetics
  • Anemia, Neonatal / therapy
  • Blood Transfusion
  • Diagnosis, Differential
  • Female
  • Gestational Age
  • Hemoglobins / analysis
  • Humans
  • Infant
  • Infant, Newborn
  • Mutation*
  • Pyruvate Kinase / deficiency*
  • Pyruvate Kinase / genetics*
  • Pyruvate Metabolism, Inborn Errors / diagnosis*
  • Pyruvate Metabolism, Inborn Errors / genetics

Substances

  • Hemoglobins
  • Pyruvate Kinase

Supplementary concepts

  • Pyruvate Kinase Deficiency of Red Cells