RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58079371
T1 Hemoglobin Disorders: Overview
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58079371
RD 2024/04/23
AB Hemoglobinopathy  is  a  genetic  defect  that  causes  abnormal  structure  of  one  of  the  globin  chains  of  the  hemoglobin  molecule.  Thalassemia  is  a  genetic  defect  resulting  in  the  production  of  an  abnormally  low  quantity  of  a  given  hemoglobin  chain  or  chains.  (Table  H-2)