Homozygous sickle cell disease with coexistent hereditary spherocytosis in three siblings

J Pediatr. 1972 Feb;80(2):235-42. doi: 10.1016/s0022-3476(72)80584-5.
No abstract available

MeSH terms

  • Adult
  • Anemia, Sickle Cell / complications*
  • Anemia, Sickle Cell / genetics
  • Anemia, Sickle Cell / pathology
  • Anemia, Sickle Cell / therapy
  • Black or African American
  • Blood Protein Electrophoresis
  • Blood Transfusion
  • Child
  • Child, Preschool
  • Female
  • Fetal Hemoglobin / analysis
  • Hemolysis
  • Homozygote
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Organ Size
  • Osmotic Fragility
  • Pedigree
  • Spherocytosis, Hereditary / complications*
  • Spherocytosis, Hereditary / genetics
  • Spherocytosis, Hereditary / pathology
  • Spherocytosis, Hereditary / therapy
  • Spleen / pathology

Substances

  • Fetal Hemoglobin