RT Book, Section
A1 Friedman, Lawrence S.
A2 Papadakis, Maxine A.
A2 McPhee, Stephen J.
A2 Rabow, Michael W.
SR Print(0)
ID 1166167270
T1 Wilson Disease
T2 Current Medical Diagnosis and Treatment 2020
YR 2020
FD 2020
PB McGraw-Hill Education
PP New York, NY
SN 9781260455281
LK accessmedicine.mhmedical.com/content.aspx?aid=1166167270
RD 2022/05/22
AB ESSENTIALS  OF  DIAGNOSISRare  autosomal  recessive  disorder  that  usually  occurs  in  persons  under  age  40.Excessive  deposition  of  copper  in  the  liver  and  brain.Serum  ceruloplasmin,  the  plasma  copper-carrying  protein,  is  low.Urinary  excretion  of  copper  and  hepatic  copper  concentration  are  high.