Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family

Ann Hematol. 2011 Mar;90(3):349-51. doi: 10.1007/s00277-010-1003-4. Epub 2010 Jun 3.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Anemia, Hemolytic / complications
  • Anemia, Hemolytic / genetics
  • Anemia, Hemolytic / therapy
  • Blood Transfusion
  • Child, Preschool
  • DNA Repeat Expansion
  • Female
  • Hemoglobins, Abnormal / genetics*
  • Humans
  • Iran
  • Phenotype
  • Splenomegaly / complications
  • Splenomegaly / genetics
  • beta-Thalassemia / blood
  • beta-Thalassemia / complications
  • beta-Thalassemia / genetics*

Substances

  • Hemoglobins, Abnormal