TY  - CHAP
M1  - Book, Section
TI  - Hemochromatosis
A1  - Friedman, Lawrence S.
A2  - Papadakis, Maxine A.
A2  - McPhee, Stephen J.
A2  - Rabow, Michael W.
A2  - McQuaid, Kenneth R.
PY  - 2022
T2  - Current Medical Diagnosis & Treatment 2022
AB  - ESSENTIALS  OF  DIAGNOSISUsually  suspected  because  of  a  family  history  or  an  elevated  iron  saturation  or  serum  ferritin.Most  patients  are  asymptomatic;  the  disease  is  rarely  recognized  clinically  before  the  fifth  decade.Hepatic  abnormalities  and  cirrhosis,  heart  failure,  hypogonadism,  and  arthritis.HFE  gene  mutation  (usually  C282Y/C282Y)  is  found  in  most  cases.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accessmedicine.mhmedical.com/content.aspx?aid=1184173570
ER  -