Diverse phenotypic expression of sickle cell hemoglobin C disease in an Indian family

Ann Hematol. 2011 Mar;90(3):357-8. doi: 10.1007/s00277-010-1014-1. Epub 2010 Jun 17.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Fetal Hemoglobin / genetics
  • Hemoglobin A2 / genetics
  • Hemoglobin C / genetics
  • Hemoglobin SC Disease / blood
  • Hemoglobin SC Disease / complications
  • Hemoglobin SC Disease / genetics
  • Hemoglobin SC Disease / pathology
  • Hemoglobin SC Disease / physiopathology*
  • Hemoglobin, Sickle / genetics
  • Hepatomegaly / etiology
  • Hepatomegaly / genetics
  • Hepatomegaly / physiopathology
  • Humans
  • Humerus / pathology
  • India
  • Male
  • Osteonecrosis / etiology
  • Osteonecrosis / pathology
  • Siblings
  • Splenomegaly / etiology
  • Splenomegaly / genetics
  • Splenomegaly / physiopathology

Substances

  • Hemoglobin, Sickle
  • Hemoglobin C
  • Hemoglobin A2
  • Fetal Hemoglobin