RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164072305
T1 Hemochromatosis
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164072305
RD 2024/04/24
AB Hereditary  hemochromatosis  is  a  disorder  in  which  iron  is  significantly  absorbed  by  the  digestive  tract  and  accumulates  in  body  tissues,  which  progressively  causes  diabetes,  joint  disorders,  cardiac  arrhythmia  then  heart  failure,  hepatic  cirrhosis,  skin  color  change,  and  increased  risk  of  cancer.  Organs  commonly  affected  by  hemochromatosis  are  the  liver,  heart,  and  endocrine  glands.