Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells

Blood. 2004 May 15;103(10):3991-2. doi: 10.1182/blood-2004-01-0225.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Anemia, Hypochromic / congenital*
  • Anemia, Hypochromic / etiology
  • Anemia, Hypochromic / genetics
  • Cation Transport Proteins / deficiency*
  • Cation Transport Proteins / genetics
  • Erythroblasts / chemistry
  • Erythroblasts / cytology
  • Female
  • Homozygote
  • Humans
  • Iron-Binding Proteins / genetics

Substances

  • Cation Transport Proteins
  • Iron-Binding Proteins
  • solute carrier family 11- (proton-coupled divalent metal ion transporters), member 2