Hemoglobin C in a patient with sickle cell anemia: transfusion-acquired SC disease

Clin Biochem. 2015 Apr;48(6):463-4. doi: 10.1016/j.clinbiochem.2015.01.013. Epub 2015 Feb 4.

Authors

Mathew P Estey¹, Karina Rodriguez Capote², Vilte E Barakauskas², Gwen Clarke³, Trefor Higgins⁴

Affiliations

¹ DynaLIFE(Dx)¸ Canada; Department of Laboratory Medicine and Pathology, University of Alberta, Canada. Electronic address: [email protected].
² DynaLIFE(Dx)¸ Canada; Department of Laboratory Medicine and Pathology, University of Alberta, Canada.
³ Department of Laboratory Medicine and Pathology, University of Alberta, Canada; Canadian Blood Services, Edmonton, Canada.
⁴ DynaLIFE(Dx)¸ Canada.

PMID: 25661304
DOI: 10.1016/j.clinbiochem.2015.01.013

No abstract available

Keywords: Hemoglobin C; Hemoglobinopathy; Red cell exchange transfusion; SC disease; Sickle cell anemia.

Publication types

Letter

MeSH terms

Anemia, Sickle Cell / blood
Anemia, Sickle Cell / etiology*
Hemoglobin C / metabolism*
Humans
Transfusion Reaction*

Substances

Hemoglobin C