TURKISH NEPHROLOGY DIALYSIS AND TRANSPLANTATION JOURNAL, cilt.27, sa.3, ss.313-315, 2018 (ESCI)
Wilson disease (WD) is an autosomal recessive inherited disease caused by abnormalities of the copper-transporting protein encoding gene ATP7B. Wilson's disease can cause various types of renal involvement. We present the case of a 56-year-old male liver transplant receiver patient who had proteinuria and cellulitis.