Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual case

Clin Chim Acta. 2004 Jun;344(1-2):221-4. doi: 10.1016/j.cccn.2004.02.021.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Anemia, Hemolytic / etiology
  • Child
  • Family Health
  • Glucosephosphate Dehydrogenase Deficiency / complications*
  • Glucosephosphate Dehydrogenase Deficiency / diagnosis
  • Humans
  • Male
  • Spherocytosis, Hereditary / complications*
  • Spherocytosis, Hereditary / diagnosis